On the public citation graph

Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents

https://doi.org/10.1021/cr2003344

0 signed · 441 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1522-2675(19980909)81:9<1608::aid-hlca1608>3.0.co;2-fopenalex-snapshot

Novel Acetogenins from the Leaves ofDasymaschalon sootepense

inferredcites →https://doi.org/10.1002/0471785156.ch6openalex-snapshot

Chiral Auxiliaries Powerful for Both Enantiomer Resolution and Determination of Absolute Configuration by X‐Ray Crystallography

inferredcites →https://doi.org/10.1002/asia.201000229openalex-snapshot

Using a Combination of Magnetic Anisotropic Effects for the Configurational Assignment of Amino Alcohols

inferredcites →https://doi.org/10.1002/cbdv.200690081openalex-snapshot

Four New Compounds from the Leaves of Acer truncatum

inferredcites →https://doi.org/10.1002/chem.200500181openalex-snapshot

The Prediction of the Absolute Stereochemistry of Primary and Secondary 1,2‐Diols by 1 H NMR Spectroscopy: Principles and Applications

inferredcites →https://doi.org/10.1002/chem.200901505openalex-snapshot

The Stereochemistry of 1,2,3‐Triols Revealed by 1H NMR Spectroscopy: Principles and Applications

inferredcites →https://doi.org/10.1002/chir.10035openalex-snapshot

Determination of absolute configuration of 1,3‐diols by the modified Mosher's method using their di‐MTPA esters

inferredcites →https://doi.org/10.1002/chir.10287openalex-snapshot

Absolute configuration determination of chiral molecules in the solution state using vibrational circular dichroism

inferredcites →https://doi.org/10.1002/chir.20125openalex-snapshot

Assignment of absolute configuration of 3‐hydroxy β‐lactams by the NMR “mix and shake” method

inferredcites →https://doi.org/10.1002/chir.20399openalex-snapshot

Enantiomeric separation and determination of absolute stereochemistry of asymmetric molecules in drug discovery—Building chiral technology toolboxes

inferredcites →https://doi.org/10.1002/chir.20473openalex-snapshot

The use of X‐ray crystallography to determine absolute configuration

inferredcites →https://doi.org/10.1002/chir.20524openalex-snapshot

Determination of absolute configuration—An overview related to this Special Issue

inferredcites →https://doi.org/10.1002/chir.20889openalex-snapshot

Assignment of absolute configuration using chiral reagents and NMR spectroscopy

inferredcites →https://doi.org/10.1002/ejoc.200500404openalex-snapshot

Antimalarial Polyketide Cycloperoxides from the Marine SpongePlakortis simplex

inferredcites →https://doi.org/10.1002/ejoc.200700966openalex-snapshot

Structural Elucidation with NMR Spectroscopy: Practical Strategies for Organic Chemists

inferredcites →https://doi.org/10.1002/ejoc.201001107openalex-snapshot

The Use of a Single Derivative in the Configurational Assignment of Ketone Cyanohydrins

inferredcites →https://doi.org/10.1002/mrc.2115openalex-snapshot

The use of MPA amide for the assignment of absolute configuration of a sterically hindered cyclic secondary amine by ‘mix and shake’ NMR method

inferredcites →https://doi.org/10.1016/0014-5793(95)90057-8openalex-snapshot

Circular dichroism: Principles and applications

inferredcites →https://doi.org/10.1016/0040-4039(94)88034-4openalex-snapshot

Absolute stereostructures of altohyrtin A and its congeners, potent cytotoxic macrolides from the Okinawan marine sponge hyrtios altum

inferredcites →https://doi.org/10.1016/j.bmc.2007.05.014openalex-snapshot

Cytotoxic dibromotyrosine-derived metabolites from the sponge Aplysina gerardogreeni

inferredcites →https://doi.org/10.1016/j.bmc.2007.11.042openalex-snapshot

Alachalasins A–G, new cytochalasins from the fungus Stachybotrys charatum

inferredcites →https://doi.org/10.1016/j.bmcl.2010.07.119openalex-snapshot

Lactarane sesquiterpenoids from Lactarius subvellereus and their cytotoxicity

inferredcites →https://doi.org/10.1016/j.bmcl.2010.08.031openalex-snapshot

Unusual antimalarial meroditerpenes from tropical red macroalgae

inferredcites →https://doi.org/10.1016/j.chroma.2004.01.065openalex-snapshot

Chiral liquid chromatography contribution to the determination of the absolute configuration of enantiomers

inferredcites →https://doi.org/10.1016/j.phytochem.2005.06.006openalex-snapshot

Polar acyclic diterpenoids from Bifurcaria bifurcata (Fucales, Phaeophyta)

inferredcites →https://doi.org/10.1016/j.phytochem.2006.09.007openalex-snapshot

Bridelionosides A–F: Megastigmane glucosides from Bridelia glauca f. balansae

inferredcites →https://doi.org/10.1016/j.phytochem.2007.07.005openalex-snapshot

Cytotoxic ent-abietane diterpenes from Gelonium aequoreum

inferredcites →https://doi.org/10.1016/j.phytochem.2008.01.020openalex-snapshot

Euodionosides A–G: Megastigmane glucosides from leaves of Euodia meliaefolia

inferredcites →https://doi.org/10.1016/j.phytochem.2010.01.004openalex-snapshot

Microtropiosides A–F: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae)

inferredcites →https://doi.org/10.1016/j.pnmrs.2010.07.003openalex-snapshot

Using NMR spectroscopic methods to determine enantiomeric purity and assign absolute stereochemistry

inferredcites →https://doi.org/10.1016/j.steroids.2006.09.005openalex-snapshot

Two novel C29-5β-sterols from the stems of Opuntia dillenii

inferredcites →https://doi.org/10.1016/j.tet.2004.07.105openalex-snapshot

The absolute stereochemistry of anachelins, siderophores from the cyanobacterium Anabaena cylindrica

inferredcites →https://doi.org/10.1016/j.tet.2004.11.039openalex-snapshot

Bioactive steroidal glycosides from the marine sponge Erylus lendenfeldi

inferredcites →https://doi.org/10.1016/j.tet.2006.06.089openalex-snapshot

Five new isocoumarins from Sonoran desert plant-associated fungal strains Paraphaeosphaeria quadriseptata and Chaetomium chiversii

inferredcites →https://doi.org/10.1016/j.tet.2007.04.081openalex-snapshot

The structures of three new shishididemniols from a tunicate of the family Didemnidae

inferredcites →https://doi.org/10.1016/j.tet.2007.07.055openalex-snapshot

Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela

inferredcites →https://doi.org/10.1016/j.tet.2007.08.095openalex-snapshot

Myrioneurinol: a novel alkaloid skeleton from Myrioneuron nutans

inferredcites →https://doi.org/10.1016/j.tet.2008.02.042openalex-snapshot

Dolastanes from the brown alga Dilophus spiralis: absolute stereochemistry and evaluation of cytotoxicity

inferredcites →https://doi.org/10.1016/j.tet.2009.02.008openalex-snapshot

Oxygenated cembranoids of the decaryiol type from the Indonesian soft coral Lobophytum sp.

inferredcites →https://doi.org/10.1016/j.tet.2009.07.005openalex-snapshot

Absolute stereochemistry and conformational analysis of achaetolide isolated from Ophiobolus sp.

inferredcites →https://doi.org/10.1016/j.tet.2009.07.019openalex-snapshot

Stereoselective synthesis and absolute configuration of the C33–C42 fragment of symbiodinolide

inferredcites →https://doi.org/10.1016/j.tet.2010.07.045openalex-snapshot

Stereocontrolled synthesis and structural confirmation of the C14–C24 degraded fragment of symbiodinolide

inferredcites →https://doi.org/10.1016/j.tet.2010.09.091openalex-snapshot

New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages

inferredcites →https://doi.org/10.1016/j.tetasy.2004.04.032openalex-snapshot

Boc–phenylglycine: a chiral solvating agent for the assignment of the absolute configuration of amino alcohols and their ethers by NMR

inferredcites →https://doi.org/10.1016/j.tetasy.2005.03.004openalex-snapshot

A straightforward route to the asymmetric synthesis of 3,4-diepipolyoxamic acid and its isomers

inferredcites →https://doi.org/10.1016/j.tetasy.2009.05.021openalex-snapshot

Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy

inferredcites →https://doi.org/10.1016/j.tetlet.2005.05.028openalex-snapshot

NMR determination of the absolute configuration of β-chiral primary alcohols

inferredcites →https://doi.org/10.1016/j.tetlet.2005.05.087openalex-snapshot

Penicillones A and B, two novel polyketides with tricyclo [5.3.1.03,8] undecane skeleton, from a marine-derived fungus Penicillium terrestre

inferredcites →https://doi.org/10.1016/j.tetlet.2008.03.027openalex-snapshot

Feroniellic acids A–C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida

inferredcites →https://doi.org/10.1016/j.tetlet.2008.11.056openalex-snapshot

Synthesis and structural determination of the C33–C42 fragment of symbiodinolide

inferredcites →https://doi.org/10.1016/j.tetlet.2009.07.014openalex-snapshot

Determination of absolute configuration of C14−C23 fragment in symbiodinolide

inferredcites →https://doi.org/10.1016/s0040-4020(01)00056-4openalex-snapshot

Determination of the absolute stereochemistry of alcohols and amines by NMR of the group directly linked to the chiral derivatizing reagent

inferredcites →https://doi.org/10.1016/s0040-4020(01)00795-5openalex-snapshot

Assignment of the absolute stereochemistry of oxazinin-1: application of the 9-AMA shift-correlation method for β-chiral primary alcohols

inferredcites →https://doi.org/10.1016/s0040-4020(97)00512-7openalex-snapshot

Determining factors in the assignment of the absolute configuration of alcohols by NMR. The use of anisotropic effects on remote positions

inferredcites →https://doi.org/10.1016/s0040-4020(98)01055-2openalex-snapshot

9-Anthrylmethoxyacetic acid esterification shifts—Correlation with the absolute stereochemistry of secondary alcohols

inferredcites →https://doi.org/10.1016/s0040-4039(00)76713-xopenalex-snapshot

Absolute stereochemistry of non-adjacent bis-tetrahydrofuranic acetogenins

inferredcites →https://doi.org/10.1016/s0040-4039(01)01724-5openalex-snapshot

Facile and purification free synthesis of Mosher amides utilizing a ROMPgel supported reagent

inferredcites →https://doi.org/10.1016/s0040-4039(96)01465-7openalex-snapshot

Absolute stereochemistry of penaresidins A and B

inferredcites →https://doi.org/10.1016/s0957-4166(00)00228-7openalex-snapshot

The assignment of absolute configurations by NMR of arylmethoxyacetate derivatives: is this methodology being correctly used?

inferredcites →https://doi.org/10.1016/s0957-4166(02)00209-4openalex-snapshot

Incorrect procedure for the assignment of the absolute configuration of carbonucleosides by NMR: MPA must not be used with primary alcohols

inferredcites →https://doi.org/10.1016/s0968-0896(96)00264-7openalex-snapshot

Additional bioactive annonaceous acetogenins from Asimina triloba (Annonaceae)

inferredcites →https://doi.org/10.1016/s0968-0896(98)00018-2openalex-snapshot

Three new bioactive bis-adjacent THF-ring acetogenins from the bark of Annona squamosa

inferredcites →https://doi.org/10.1021/cr000407mopenalex-snapshot

Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary Perspective

inferredcites →https://doi.org/10.1021/cr000414aopenalex-snapshot

Recent Advances in the Synthesis of Sialic Acid Derivatives and Sialylmimetics as Biological Probes

inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot

The Assignment of Absolute Configuration by NMR

inferredcites →https://doi.org/10.1021/cr030733copenalex-snapshot

Determination of Relative Configuration in Organic Compounds by NMR Spectroscopy and Computational Methods

inferredcites →https://doi.org/10.1021/ja00105a078openalex-snapshot

Relative and Absolute Stereochemistry of Pyripyropene A, A Potent, Bioavailable Inhibitor of Acyl-CoA:Cholesterol Acyltransferase (ACAT)

inferredcites →https://doi.org/10.1021/ja004154qopenalex-snapshot

Toward Creation of a Universal NMR Database for Stereochemical Assignment: Complete Structure of the Desertomycin/Oasomycin Class of Natural Products

inferredcites →https://doi.org/10.1021/ja0375481openalex-snapshot

Universal NMR Databases for Contiguous Polyols

inferredcites →https://doi.org/10.1021/ja0558948openalex-snapshot

Marinomycins A−D, Antitumor-Antibiotics of a New Structure Class from a Marine Actinomycete of the Recently Discovered Genus “ Marinispora ”

inferredcites →https://doi.org/10.1021/ja062469lopenalex-snapshot

On the Proof and Disproof of Natural Product Stereostructures: Characterization and Analysis of a Twenty-Eight Member Stereoisomer Library of Murisolins and Their Mosher Ester Derivatives

inferredcites →https://doi.org/10.1021/ja900849fopenalex-snapshot

A “Shortcut” Mosher Ester Method To Assign Configurations of Stereocenters in Nearly Symmetric Environments. Fluorous Mixture Synthesis and Structure Assignment of Petrocortyne A

inferredcites →https://doi.org/10.1021/ja9700055openalex-snapshot

Are Both the (R)- and the (S)-MPA Esters Really Needed for the Assignment of the Absolute Configuration of Secondary Alcohols by NMR? The Use of a Single Derivative

inferredcites →https://doi.org/10.1021/ja973159topenalex-snapshot

Solid-State Nuclear Magnetic Resonance Spectroscopic and Quantum Chemical Investigation of 13C and 17O Chemical Shift Tensors, 17O Nuclear Quadrupole Coupling Tensors, and Bonding in Transition-Metal Carbonyl Complexes and Clusters

inferredcites →https://doi.org/10.1021/jo00043a018openalex-snapshot

The natural polypropionate-derived esters of the mollusk Onchidium sp

inferredcites →https://doi.org/10.1021/jo00094a035openalex-snapshot

On the Use of O-Methylmandelic Acid for the Establishment of Absolute Configuration of .alpha.-Chiral Primary Amines

inferredcites →https://doi.org/10.1021/jo00108a008openalex-snapshot

Conformational Structure and Dynamics of Arylmethoxyacetates: DNMR Spectroscopy and Aromatic Shielding Effect

inferredcites →https://doi.org/10.1021/jo00111a011openalex-snapshot

Determination of the Absolute Stereochemistry of Chiral Amines by 1H NMR of Arylmethoxyacetic Acid Amides: The Conformational Model

inferredcites →https://doi.org/10.1021/jo020240sopenalex-snapshot

Structure and Absolute Stereochemistry of Phormidolide, a New Toxic Metabolite from the Marine Cyanobacterium Phormidium sp.

inferredcites →https://doi.org/10.1021/jo0256989openalex-snapshot

Absolute Configuration of Secondary Alcohols by 1H NMR: In Situ Complexation of α-Methoxyphenylacetic Acid Esters with Barium(II)

inferredcites →https://doi.org/10.1021/jo0343634openalex-snapshot

Amphidinolide X, a Novel 16-Membered Macrodiolide from Dinoflagellate Amphidinium sp.

inferredcites →https://doi.org/10.1021/jo048029zopenalex-snapshot

Automatic Assignment of Absolute Configuration from 1D NMR Data

inferredcites →https://doi.org/10.1021/jo048643aopenalex-snapshot

Determining the Absolute Stereochemistry of Secondary/Secondary Diols by 1H NMR: Basis and Applications

inferredcites →https://doi.org/10.1021/jo0522207openalex-snapshot

Role of Barium(II) in the Determination of the Absolute Configuration of Chiral Amines by 1H NMR Spectroscopy

inferredcites →https://doi.org/10.1021/jo060958yopenalex-snapshot

Cytotoxic Macrolides from a New Species of the Deep-Water Marine Sponge Leiodermatium

inferredcites →https://doi.org/10.1021/jo061878xopenalex-snapshot

Arenicolides A−C, 26-Membered Ring Macrolides from the Marine Actinomycete Salinispora arenicola

inferredcites →https://doi.org/10.1021/jo061939ropenalex-snapshot

Relative and Absolute Stereochemistry of Secondary/Secondary Diols: Low-Temperature 1H NMR of Their bis-MPA Esters

inferredcites →https://doi.org/10.1021/jo062013mopenalex-snapshot

Complete Structure Elucidation of Shishididemniols, Complex Lipids with Tyramine-Derived Tether and Two Serinol Units, from a Marine Tunicate of the Family Didemnidae

inferredcites →https://doi.org/10.1021/jo062097zopenalex-snapshot

The Assignment of the Absolute Configuration of Diethyl Hydroxy- and Aminophosphonates by1H and31P NMR Using Naproxen as a Reliable Chiral Derivatizing Agent

inferredcites →https://doi.org/10.1021/jo070278aopenalex-snapshot

1-Benzotriazol-1-yl-3,3,3-trifluoro-2-methoxy-2- phenylpropan-1-ones: Mosher-Bt Reagents

inferredcites →https://doi.org/10.1021/jo070414bopenalex-snapshot

Iriomoteolide-1a, a Potent Cytotoxic 20-Membered Macrolide from a Benthic Dinoflagellate Amphidinium Species

inferredcites →https://doi.org/10.1021/jo702440sopenalex-snapshot

Iriomoteolide-3a, a Cytotoxic 15-Membered Macrolide from a Marine Dinoflagellate Amphidinium Species

inferredcites →https://doi.org/10.1021/jo800469copenalex-snapshot

Resin-Bound Chiral Derivatizing Agents for Assignment of Configuration by NMR Spectroscopy

inferredcites →https://doi.org/10.1021/jo8019187openalex-snapshot

Simple Chiral Derivatization Protocols for 1H NMR and 19F NMR Spectroscopic Analysis of the Enantiopurity of Chiral Diols

inferredcites →https://doi.org/10.1021/jo801944dopenalex-snapshot

Marinisporolides, Polyene-Polyol Macrolides from a Marine Actinomycete of the New Genus Marinispora

inferredcites →https://doi.org/10.1021/jo900546kopenalex-snapshot

Synthesis and Structural Revision of Symbiodinolide C23−C34 Fragment

inferredcites →https://doi.org/10.1021/jo960719iopenalex-snapshot

MTPA vs MPA in the Determination of the Absolute Configuration of Chiral Alcohols by 1H NMR

inferredcites →https://doi.org/10.1021/jo970427xopenalex-snapshot

Choosing the Right Reagent for the Determination of the Absolute Configuration of Amines by NMR: MTPA or MPA?

inferredcites →https://doi.org/10.1021/jo980409vopenalex-snapshot

Determination of Absolute Configurations of Carbinols of Annonaceous Acetogenins with 2-Naphthylmethoxyacetic Acid Esters

inferredcites →https://doi.org/10.1021/np0497797openalex-snapshot

A Cytotoxic Carotenoid from the Marine Sponge Prianos osiros

inferredcites →https://doi.org/10.1021/np0501583openalex-snapshot

Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B

inferredcites →https://doi.org/10.1021/np0700570openalex-snapshot

Cytotoxic Germacranolides and Acyclic Diterpenoides from the Seeds of Carpesium triste

inferredcites →https://doi.org/10.1021/np070539bopenalex-snapshot

Novel Open-Chain Cytochalsins from the Marine-Derived Fungus Spicaria elegans

inferredcites →https://doi.org/10.1021/np50124a009openalex-snapshot

Asimilobin and cis- and trans-Murisolinones, Novel Bioactive Annonaceous Acetogenins from the Seeds of Asimina triloba

inferredcites →https://doi.org/10.1021/np800095gopenalex-snapshot

Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi

inferredcites →https://doi.org/10.1021/np900449ropenalex-snapshot

ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound

inferredcites →https://doi.org/10.1021/np9605448openalex-snapshot

New Type of Mono-tetrahydrofuran Ring Acetogenins from Goniothalamus donnaiensis

inferredcites →https://doi.org/10.1021/np9701283openalex-snapshot

Novel Mono-Tetrahydrofuran Ring Acetogenins, from the Bark of Annona squamosa, Showing Cytotoxic Selectivities for the Human Pancreatic Carcinoma Cell Line, PACA-2

inferredcites →https://doi.org/10.1021/ol0062852openalex-snapshot

Absolute Configuration of 1,n-Diols by NMR: The Importance of the Combined Anisotropic Effects in Bis-Arylmethoxyacetates

inferredcites →https://doi.org/10.1021/ol010108zopenalex-snapshot

Toward the Creation of NMR Databases in Chiral Solvents for Assignments of Relative and Absolute Stereochemistry: Proof of Concept

inferredcites →https://doi.org/10.1021/ol010109ropenalex-snapshot

Toward the Creation of NMR Databases in Chiral Solvents for Assignments of Relative and Absolute Stereochemistry: Scope and Limitation

inferredcites →https://doi.org/10.1021/ol010110qopenalex-snapshot

Toward the Creation of NMR Databases in Chiral Solvents for Assignments of Relative and Absolute Stereochemistry: NMR Desymmetrization of Meso Compounds

inferredcites →https://doi.org/10.1021/ol0171160openalex-snapshot

Toward the Creation of NMR Databases in Chiral Solvents: Bidentate Chiral NMR Solvents for Assignment of the Absolute Configuration of Acyclic Secondary Alcohols

inferredcites →https://doi.org/10.1021/ol025759popenalex-snapshot

Caylobolide A, a Unique 36-Membered Macrolactone from a Bahamian Lyngbya majuscula

inferredcites →https://doi.org/10.1021/ol034853iopenalex-snapshot

“Mix and Shake” Method for Configurational Assignment by NMR: Application to Chiral Amines and Alcohols

inferredcites →https://doi.org/10.1021/ol051764sopenalex-snapshot

The Assignment of the Absolute Configuration of 1,2-Diols by Low-Temperature NMR of a Single MPA Derivative

inferredcites →https://doi.org/10.1021/ol052686bopenalex-snapshot

Cyanosporasides A and B, Chloro- and Cyano-cyclopenta[ a ]indene Glycosides from the Marine Actinomycete “ Salinispora pacifica ”

inferredcites →https://doi.org/10.1021/ol0616135openalex-snapshot

The 1H NMR Method for the Determination of the Absolute Configuration of 1,2,3-prim,sec,sec-Triols

inferredcites →https://doi.org/10.1021/ol070510zopenalex-snapshot

Isolation and Characterization of Biogenetically Related Highly Oxygenated Nortriterpenoids from Schisandra chinensis

inferredcites →https://doi.org/10.1021/ol071382hopenalex-snapshot

More than a Protective Group: Synthesis and Applications of a New Chiral Silane

inferredcites →https://doi.org/10.1021/ol1003862openalex-snapshot

Long-Range Shielding Effects in the 1H NMR Spectra of Mosher-like Ester Derivatives

inferredcites →https://doi.org/10.1021/ol7017455openalex-snapshot

N-(2-Nitrophenyl)proline: An Intramolecular Hydrogen Bond Forming Reagent for the Determination of the Absolute Configuration of Primary Amines

inferredcites →https://doi.org/10.1021/ol7022196openalex-snapshot

Chiral Thiols: The Assignment of Their Absolute Configuration by 1H NMR

inferredcites →https://doi.org/10.1021/ol8008528openalex-snapshot

Cross Interaction Between Auxiliaries: The Chirality of Amino Alcohols by NMR

inferredcites →https://doi.org/10.1021/ol800853uopenalex-snapshot

Assigning the Configuration of Amino Alcohols by NMR: A Single Derivatization Method

inferredcites →https://doi.org/10.1021/ol8023314openalex-snapshot

Absolute Configuration of Ketone Cyanohydrins by 1H NMR: The Special Case of Polar Substituted Tertiary Alcohols

inferredcites →https://doi.org/10.1021/ol802709xopenalex-snapshot

Mycangimycin, a Polyene Peroxide from a Mutualist Streptomyces sp.

inferredcites →https://doi.org/10.1021/ol9021639openalex-snapshot

Chiral 1,2-Diols: The Assignment of Their Absolute Configuration by NMR Made Easy

inferredcites →https://doi.org/10.1038/363418a0openalex-snapshot

Rational design of potent sialidase-based inhibitors of influenza virus replication

inferredcites →https://doi.org/10.1039/a809629eopenalex-snapshot

Chiroptical methods in the stereochemical analysis of natural products (1975 to 1999)

inferredcites →https://doi.org/10.1039/b202823aopenalex-snapshot

Synthesis of (+)-polyoxamic acid and D-sorbitol from simple achiral allylic halides employing (S,S)-hydrobenzoin as a chiral source

inferredcites →https://doi.org/10.1039/b510806copenalex-snapshot

Absolute configuration of amino alcohols by 1H-NMR

inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot

Application of electronic circular dichroism in configurational and conformational analysis of organic compounds

inferredcites →https://doi.org/10.1039/b617184bopenalex-snapshot

Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: application to chiral primary alcohols

inferredcites →https://doi.org/10.1039/b707989nopenalex-snapshot

New methods for stereochemical determination of complex polyketides: configurational assignment of novel metabolites from myxobacteria

inferredcites →https://doi.org/10.1039/b806529bopenalex-snapshot

In tube determination of the absolute configuration of α- and β-hydroxy acids by NMR via chiral BINOL borates

inferredcites →https://doi.org/10.1039/c0cc02774jopenalex-snapshot

13C NMR as a general tool for the assignment of absolute configuration

inferredcites →https://doi.org/10.1080/03639040701662677openalex-snapshot

Discrimination of Chiral Compounds Using NMR Spectroscopy

inferredcites →https://doi.org/10.1246/bcsj.79.965openalex-snapshot

The Modified Mosher’s Method and the Sulfoximine Method

inferredcites →https://doi.org/10.1248/cpb.55.137openalex-snapshot

Two New Stereoisomers of Tetrahydrofuranoid Lignans from the Flower Buds of Magnolia fargesii

inferredcites →https://doi.org/10.1248/cpb.55.1600openalex-snapshot

Tricalysiosides P-U: Ent-kaurane Glucosides and a Labdane Glucoside from Leaves of Tricalysia dubia OHWI

inferredcites →https://doi.org/10.1248/cpb.55.1720openalex-snapshot

Glycolipids from the Formosan Soft Coral Lobophytum crassum

inferredcites →https://doi.org/10.1248/cpb.56.547openalex-snapshot

Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis

inferredcites →https://doi.org/10.1248/cpb.57.863openalex-snapshot

Two New Phenylglycol Derivatives Isolated from Syringa reticulata var. mandshurica and Their Antifungal Activities

inferredcites →https://doi.org/10.1271/bbb.61.881openalex-snapshot

Absolute Configurations of Some Hydroxy-fatty Acids Produced by the Insect Genus Laccifer

inferredcites →https://doi.org/10.1271/bbb.80457openalex-snapshot

Inconspicamide, New N -Acylated Serinol from the Marine Sponge Stelletta inconspicua

inferredcites →https://doi.org/10.1517/14656566.4.5.799openalex-snapshot

Zanamivir in the treatment of influenza

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112929zenodo-depositor-declared

Specialised metabolites as chemotaxonomic markers of Coptosapelta diffusa, supporting its delimitation as sisterhood phylogenetic relationships with Rubioideae

inferred← citeshttps://doi.org/10.1002/9780470034590.emrstm1398openalex-snapshot

NMR Methods for the Assignment of Absolute Stereochemistry of Bioactive Compounds

inferred← citeshttps://doi.org/10.1002/9781118876015.ch5openalex-snapshot

Emerging Trends for Stimulating the Discovery of Natural Products

inferred← citeshttps://doi.org/10.1002/9783527664610.ch7openalex-snapshot

Simplified NMR Procedures for the Assignment of the Absolute Configuration

inferred← citeshttps://doi.org/10.1002/ajoc.202200544openalex-snapshot

Chiral Analysis of Pharmaceuticals Using NMR Spectroscopy: A Review

inferred← citeshttps://doi.org/10.1002/ange.201203406openalex-snapshot

Total Synthesis of the Nominal Didemnaketal A

inferred← citeshttps://doi.org/10.1002/ange.202405860openalex-snapshot

Discovery, Total Synthesis, and Anti‐Inflammatory Evaluation of Naturally Occurring Naphthopyrone‐Macrolide Hybrids as Potent NLRP3 Inflammasome Inhibitors

inferred← citeshttps://doi.org/10.1002/anie.201203406openalex-snapshot

Total Synthesis of the Nominal Didemnaketal A

inferred← citeshttps://doi.org/10.1002/anie.202004992openalex-snapshot

Absolute Configuration of Small Molecules by Co‐Crystallization

inferred← citeshttps://doi.org/10.1002/anie.202405860openalex-snapshot

Discovery, Total Synthesis, and Anti‐Inflammatory Evaluation of Naturally Occurring Naphthopyrone‐Macrolide Hybrids as Potent NLRP3 Inflammasome Inhibitors

inferred← citeshttps://doi.org/10.1002/ansa.202300021openalex-snapshot

Analysis of isomeric mixtures by molecular rotational resonance spectroscopy

inferred← citeshttps://doi.org/10.1002/cbdv.202300005openalex-snapshot

The Inhibitory Activity of Natural Products to Xanthine Oxidase

inferred← citeshttps://doi.org/10.1002/cbic.201402306openalex-snapshot

Synergistic Actions of Tailoring Enzymes in Pradimicin Biosynthesis

inferred← citeshttps://doi.org/10.1002/chem.201404291openalex-snapshot

Structure and Biosynthetic Assembly of Gulmirecins, Macrolide Antibiotics from the Predatory Bacterium Pyxidicoccus fallax

inferred← citeshttps://doi.org/10.1002/chem.201601064openalex-snapshot

Host–Guest Assembly of a Molecular Reporter with Chiral Cyanohydrins for Assignment of Absolute Stereochemistry

inferred← citeshttps://doi.org/10.1002/chem.201602884openalex-snapshot

Design of Selenium‐Based Chiral Chemical Probes for Simultaneous Enantio‐ and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy

inferred← citeshttps://doi.org/10.1002/chem.201704928openalex-snapshot

The Rickiols: 20‐, 22‐, and 24‐membered Macrolides from the Ascomycete Hypoxylon rickii

inferred← citeshttps://doi.org/10.1002/chem.202000870openalex-snapshot

Pyrrole‐Protected β‐Aminoalkylzinc Reagents for the Enantioselective Synthesis of Amino‐Derivatives

inferred← citeshttps://doi.org/10.1002/chem.202203970openalex-snapshot

Absolute Configuration Determination of Chiral API Molecules by MicroED Analysis of Cocrystal Powders Formed Based on Cocrystal Propensity Prediction Calculations**

inferred← citeshttps://doi.org/10.1002/chin.201240280openalex-snapshot

ChemInform Abstract: Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents

inferred← citeshttps://doi.org/10.1002/chir.20628openalex-snapshot

Importance of hydrogen‐bonding sites in the chiral recognition mechanism between racemic D3 terbium(III) complexes and amino acids

inferred← citeshttps://doi.org/10.1002/chir.22182openalex-snapshot

Application of NMR spectroscopy for assignment of the absolute configuration of 8‐tert‐butyl‐2‐hydroxy‐7‐methoxy‐8‐methyl‐9‐oxa‐6‐azaspiro[4.5]dec‐6‐en‐10‐one

inferred← citeshttps://doi.org/10.1002/chir.22221openalex-snapshot

Cooperative Use of VCD and XRD for the Determination of Tetrahydrobenzoisoquinolines Absolute Configuration: A Reliable Proof of Memory of Chirality and Retention of Configuration in Enediyne Rearrangements

inferred← citeshttps://doi.org/10.1002/chir.22315openalex-snapshot

Enantiopure O‐Ethyl Phenylphosphonothioic Acid: A Solvating Agent for the Determination of Enantiomeric Excesses

inferred← citeshttps://doi.org/10.1002/chir.22319openalex-snapshot

Lanthanide Tris(β‐diketonates) as Useful Probes for Chirality Determination of Biological Amino Alcohols in Vibrational Circular Dichroism: Ligand to Ligand Chirality Transfer in Lanthanide Coordination Sphere

inferred← citeshttps://doi.org/10.1002/chir.22491openalex-snapshot

Utilization of (18‐Crown‐6)‐2,3,11,12‐tetracarboxylic Acid as a Chiral NMR Solvating Agent for Diamines and β‐Amino Acids

inferred← citeshttps://doi.org/10.1002/chir.22558openalex-snapshot

Stereochemistry of the Brivaracetam Diastereoisomers

inferred← citeshttps://doi.org/10.1002/chir.22582openalex-snapshot

Synthesis and Utilization of Trialkylammonium‐Substituted Cyclodextrins as Water‐Soluble Chiral NMR Solvating Agents for Anionic Compounds

inferred← citeshttps://doi.org/10.1002/chir.23030openalex-snapshot

NMR chiral discrimination of chalcogen containing secondary alcohols

inferred← citeshttps://doi.org/10.1002/cplu.201800493openalex-snapshot

2H and 13C NMR‐Based Enantiodetection Using Polyacetylene versus Polypeptide Aligning Media: Versatile and Complementary Tools for Chemists

inferred← citeshttps://doi.org/10.1002/ejoc.201403582openalex-snapshot

First Total Synthesis of Piperenol B and Configuration Revision of the Enantiomers Piperenol B and Uvarirufol A

inferred← citeshttps://doi.org/10.1002/ejoc.201601068openalex-snapshot

TADDOL‐Promoted Enantioselective Intramolecular Diels–Alder Reactions of 1,7,9‐Decatrien‐3‐ones to Octalin Derivatives

inferred← citeshttps://doi.org/10.1002/ejoc.201800689openalex-snapshot

An Improved Synthesis of the Antibiotic Dehydrophos

inferred← citeshttps://doi.org/10.1002/ejoc.202000396openalex-snapshot

Arylboronic Acids and their Myriad of Applications Beyond Organic Synthesis

inferred← citeshttps://doi.org/10.1002/ejoc.202101104openalex-snapshot

Synthetic Studies on Alotamide A: Construction of N‐Demethylalotamide A

inferred← citeshttps://doi.org/10.1002/hlca.202000081openalex-snapshot

Chiral α‐Amino Acid‐Based NMR Solvating Agents

inferred← citeshttps://doi.org/10.1002/mrc.4167openalex-snapshot

Chiral discrimination of secondary alcohols and carboxylic acids by NMR spectroscopy

inferred← citeshttps://doi.org/10.1002/mrc.4192openalex-snapshot

The determination of the absolute configuration of a chiral 2,3′‐diindolylarylmethane by NMR spectroscopy

inferred← citeshttps://doi.org/10.1002/mrc.4322openalex-snapshot

Improving the performance of J‐modulated ADEQUATE experiments through homonuclear decoupling and non‐uniform sampling

inferred← citeshttps://doi.org/10.1002/mrc.4634openalex-snapshot

Multiple homonuclear band‐selective decoupling NMR : Fast and unambiguous determination of diastereomeric excess

inferred← citeshttps://doi.org/10.1002/wcms.1214openalex-snapshot

Addressing the stereochemistry of complex organic molecules by density functional theory‐ NMR

inferred← citeshttps://doi.org/10.1007/128_2013_433openalex-snapshot

Chiral Derivatizing Agents, Macrocycles, Metal Complexes, and Liquid Crystals for Enantiomer Differentiation in NMR Spectroscopy

inferred← citeshttps://doi.org/10.1007/12_2013_260openalex-snapshot

Helical Polymer–Metal Complexes: The Role of Metal Ions on the Helicity and the Supramolecular Architecture of Poly(phenylacetylene)s

inferred← citeshttps://doi.org/10.1007/978-3-032-20497-4_5openalex-snapshot

Chirality Discrimination Using Chiral Derivatizing Agents

inferred← citeshttps://doi.org/10.1007/978-3-032-20497-4_7openalex-snapshot

Chiral Recognition Using 31P-NMR Spectra

inferred← citeshttps://doi.org/10.1007/s00216-007-1577-4openalex-snapshot

High-precision frequency measurements: indispensable tools at the core of the molecular-level analysis of complex systems

inferred← citeshttps://doi.org/10.1007/s00253-024-13235-xopenalex-snapshot

Catabolism of 2-keto-3-deoxy-galactonate and the production of its enantiomers

inferred← citeshttps://doi.org/10.1007/s00726-018-2653-0openalex-snapshot

1H NMR spectroscopy in the presence of Mosher acid to rapidly determine the enantiomeric composition of amino acid benzyl esters, chirons susceptible to easy racemization

inferred← citeshttps://doi.org/10.1007/s11274-019-2707-9openalex-snapshot

Virgicin, a novel lanthipeptide from Virgibacillus sp. strain AK90 exhibits inhibitory activity against Gram-positive bacteria

inferred← citeshttps://doi.org/10.1007/s11426-024-1989-yopenalex-snapshot

Increase of chiral sensing ability in host-guest chemistry by magnetic anisotropy

inferred← citeshttps://doi.org/10.1007/s13659-025-00579-8openalex-snapshot

Polydosetins & pullularins—bioactive tetramic acids & cyclodepsipeptides from the endophytic and nematophagous fungus Polydomus karssenii

inferred← citeshttps://doi.org/10.1007/s40242-024-4011-yopenalex-snapshot

A Concise, Practical Chiral Resolution Approach of Racemic (E)-4,4-Dimethyl-1-(4-nitrophenyl)pent-1-en-3-ol to Its both Enantiomers via Strategy of Diastereomeric Ester Formation and Crystallization Using both N-Boc-D- and N-Boc-L-phenylglycines as Chiral Auxiliaries

inferred← citeshttps://doi.org/10.1007/s42995-021-00125-8openalex-snapshot

Linear polyketides produced by co-culture of Penicillium crustosum and Penicillium fellutanum

inferred← citeshttps://doi.org/10.1007/s42995-023-00173-2openalex-snapshot

Isolation and characterization of three pairs of verrucosidin epimers from the marine sediment-derived fungus Penicillium cyclopium and configuration revision of penicyrone A and related analogues

inferred← citeshttps://doi.org/10.1007/s43450-021-00184-zopenalex-snapshot

Vibrational Circular Dichroism for the Assignment of Absolute Configuration of Natural Products in Brazil

inferred← citeshttps://doi.org/10.1007/s43450-022-00333-yopenalex-snapshot

From Relative to Absolute Stereochemistry of Secondary Metabolites: Applications in Plant Chemistry

inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12115-8openalex-snapshot

Absolute Stereochemistry by NMR Spectroscopy

inferred← citeshttps://doi.org/10.1016/b978-0-12-821062-8.00008-9openalex-snapshot

Configurational analysis

inferred← citeshttps://doi.org/10.1016/b978-0-444-63359-0.00007-0openalex-snapshot

Nuclear Magnetic Resonance Spectroscopy for Structural Characterization of Bioactive Compounds

inferred← citeshttps://doi.org/10.1016/b978-0-444-64027-7.00008-2openalex-snapshot

Chiroptical Probes for Determination of Absolute Stereochemistry by Circular Dichroism Exciton Chirality Method

inferred← citeshttps://doi.org/10.1016/b978-0-444-64027-7.00009-4openalex-snapshot

Chiral Analysis by NMR Spectroscopy: Chiral Solvating Agents

inferred← citeshttps://doi.org/10.1016/bs.arnmr.2016.12.001openalex-snapshot

Novel Synthetic As Well As Natural Auxiliaries With a Blend of NMR Methodological Developments for Chiral Analysis in Isotropic Media

inferred← citeshttps://doi.org/10.1016/j.apsb.2026.05.005openalex-snapshot

Bispericyclase guided discovery of nargenicin-type natural products

inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.12.008openalex-snapshot

Xanthine oxidase inhibitors from an endophytic fungus Lasiodiplodia pseudotheobromae

inferred← citeshttps://doi.org/10.1016/j.bmc.2017.01.048openalex-snapshot

An epigenetic modifier induces production of (10′S)-verruculide B, an inhibitor of protein tyrosine phosphatases by Phoma sp. nov. LG0217, a fungal endophyte of Parkinsonia microphylla

inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.06.072openalex-snapshot

Lipid-lowering polyketides from a soft coral-derived fungus Cladosporium sp. TZP29

inferred← citeshttps://doi.org/10.1016/j.chempr.2022.12.006openalex-snapshot

First trans-eunicellane terpene synthase in bacteria

inferred← citeshttps://doi.org/10.1016/j.cplett.2015.02.016openalex-snapshot

CH-RES-TOCSY: Enantiomers spectral resolution and measurement of heteronuclear residual dipolar couplings

inferred← citeshttps://doi.org/10.1016/j.enzmictec.2018.07.004openalex-snapshot

Progress in using threonine aldolases for preparative synthesis

inferred← citeshttps://doi.org/10.1016/j.fitote.2016.06.011openalex-snapshot

Adeninealkylresorcinol, the first alkylresorcinol tethered with nucleobase from Lasiodiplodia sp.

inferred← citeshttps://doi.org/10.1016/j.fitote.2016.11.008openalex-snapshot

Antimicrobial metabolites from the plant endophytic fungus Penicillium sp.

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105387openalex-snapshot

Five new verrucosidin derivatives from Penicillium polonicum, a deep-sea cold-seep sediment isolated fungus

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.09.210openalex-snapshot

New flexible cembrane-type macrocyclic diterpenes as TNF-α inhibitors from the South China Sea soft coral Sarcophyton mililatensis

inferred← citeshttps://doi.org/10.1016/j.isci.2019.07.051openalex-snapshot

A Gallium-based Chiral Solvating Agent Enables the Use of 1H NMR Spectroscopy to Differentiate Chiral Alcohols

inferred← citeshttps://doi.org/10.1016/j.jpba.2017.02.037openalex-snapshot

Application of Mosher’s method for absolute configuration assignment to bioactive plants and fungi metabolites

inferred← citeshttps://doi.org/10.1016/j.jpba.2017.07.008openalex-snapshot

The market of chiral drugs: Chiral switches versus de novo enantiomerically pure compounds

inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.04.007openalex-snapshot

Minor oxygenated cannabinoids from high potency Cannabis sativa L.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113200openalex-snapshot

Polychlorinated cyclopentenes from a marine derived Periconia sp. (strain G1144)

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113902openalex-snapshot

Characteristic chromanone acids from Calophyllum membranaceum: Determination of C-3 configuration and anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.phytol.2013.03.009openalex-snapshot

Two new dihydrobenzofuran-type neolignans from Breynia fruticosa

inferred← citeshttps://doi.org/10.1016/j.pnmrs.2019.10.001openalex-snapshot

Multinuclear NMR in polypeptide liquid crystals: Three fertile decades of methodological developments and analytical challenges

inferred← citeshttps://doi.org/10.1016/j.snb.2016.03.002openalex-snapshot

A bisthiourea-based 1 H NMR chiral sensor for chiral discrimination of a variety of chiral compounds

inferred← citeshttps://doi.org/10.1016/j.tet.2010.03.093openalex-snapshot

Total synthesis of (+)-papulacandin D

inferred← citeshttps://doi.org/10.1016/j.tet.2011.04.051openalex-snapshot

Isolation and characterization of actinoramides A–C, highly modified peptides from a marine Streptomyces sp.

inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.106openalex-snapshot

Biosynthesis of the apoptolidins in Nocardiopsis sp. FU 40

inferred← citeshttps://doi.org/10.1016/j.tet.2011.12.070openalex-snapshot

Integrated approaches to the configurational assignment of marine natural products

inferred← citeshttps://doi.org/10.1016/j.tet.2013.10.077openalex-snapshot

Designing chiral derivatizing agents (CDA) for the NMR assignment of the absolute configuration: a theoretical and experimental approach with thiols as a case study

inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.057openalex-snapshot

Stereochemical investigation and total synthesis of inuloidin, a biologically active sesquiterpenoid from Heterotheca inuloides

inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.052openalex-snapshot

Synthesis of optically pure γPNA monomers: a comparative study

inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.06.012openalex-snapshot

FICA, a new chiral derivatizing agent for determining the absolute configuration of secondary alcohols by 19F and 1H NMR spectroscopies

inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.11.014openalex-snapshot

Enantiodifferentiation of multifunctional tertiary alcohols by NMR spectroscopy with a Whelk-O type chiral solvating agent

inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.12.011openalex-snapshot

Determination of absolute configuration by 31P NMR

inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.01.004openalex-snapshot

Assignment of the absolute configuration of hydroxy acids using 1H NMR spectroscopy: a simple and rapid approach

inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.09.002openalex-snapshot

Ferrocene derivatives of liquid chiral molecules allow assignment of absolute configuration by X-ray crystallography

inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.09.009openalex-snapshot

Strategies for using NMR spectroscopy to determine absolute configuration

inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.09.017openalex-snapshot

Some new protocols for the assignment of absolute configuration by NMR spectroscopy using chiral solvating agents and CDAs

inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.10.010openalex-snapshot

Lipase-catalyzed kinetic resolution approach toward enantiomerically enriched 1-(β-hydroxypropyl)indoles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.178openalex-snapshot

Structure determination and absolute configuration of cannabichromanone derivatives from high potency Cannabis sativa

inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.014openalex-snapshot

Antioxidant sordariol dimers from Sordaria macrospora and the absolute configuration determinations of their two simultaneous linear 1,2-diols

inferred← citeshttps://doi.org/10.1016/j.xcrp.2025.103065openalex-snapshot

A unifying geometric framework for computational representation of stereoisomers based on mixed product

inferred← citeshttps://doi.org/10.1016/s1875-5364(13)60016-3openalex-snapshot

Determination of the absolute configuration of natural products

inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00650openalex-snapshot

Absolute Stereochemical Determination of Organic Molecules through Induction of Helicity in Host–Guest Complexes

inferred← citeshttps://doi.org/10.1021/acs.analchem.1c03783openalex-snapshot

Construction of Lewis Pairs for Optimal Enantioresolution via Recognition-Enabled “Chromatographic” 19F NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.analchem.3c05395openalex-snapshot

Chiral Recognition of Chiral (Hetero)Cyclic Derivatives Probed by Tetraaza Macrocyclic Chiral Solvating Agents via 1H NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.analchem.5b01288openalex-snapshot

Precise Determination of Enantiomeric Excess by a Sensitivity Enhanced Two-Dimensional Band-Selective Pure-Shift NMR

inferred← citeshttps://doi.org/10.1021/acs.analchem.5c04345openalex-snapshot

A 19F-Labeled Isothiocyanate Derivatizing Agent for the Chiral Discrimination of Cyclic Secondary Amines

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c04091openalex-snapshot

Praseodymium Metallacrown-Based NMR Probe for Enantioselective Discrimination of Mandelate Anions in Water

inferred← citeshttps://doi.org/10.1021/acs.jafc.0c05938openalex-snapshot

Enantioselective Analysis and Degradation Studies of Four Stereoisomers of Difenoconazole in Citrus by Chiral Liquid Chromatography–Tandem Mass Spectrometry

inferred← citeshttps://doi.org/10.1021/acs.jafc.1c06253openalex-snapshot

Four Propiconazole Stereoisomers: Stereoselective Bioactivity, Separation via Liquid Chromatography–Tandem Mass Spectrometry, and Dissipation in Banana Leaves

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01309openalex-snapshot

Opportunities and Limitations for Assigning Relative Configurations of Antibacterial Bislactones using GIAO NMR Shift Calculations

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00813openalex-snapshot

Phenethoxy Derivatives with Anti-inflammatory Activities from the Betelnut Endophytic Trichoderma asperellum G10

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01179openalex-snapshot

Enigmazole C: A Cytotoxic Macrocyclic Lactone and Its Ring-Opened Derivatives from a New Species of Homophymia Sponge

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00015openalex-snapshot

Acremosides A–G, Sugar Alcohol-Conjugated Acyclic Sesquiterpenes from a Sponge-Derived Acremonium Species

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00454openalex-snapshot

Triplinones A–H: Anti-Inflammatory Arylalkenyl α,β-Unsaturated-δ-Lactones Isolated from the Leaves of Australian Rainforest Plant Cryptocarya triplinervis (Lauraceae)

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00654openalex-snapshot

Reaping the Chemical Diversity of Morinagamyces vermicularis Using Feature-Based Molecular Networking

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01445openalex-snapshot

Menominin A and B: Cytotoxic Cyclodepsipeptides from the Freshwater Sponge-Associated Cyanobacterium Nostoc sp. UIC 10607

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00519openalex-snapshot

Azaphilones from an Acid Mine Extremophile Strain of a Pleurostomophora sp.

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00690openalex-snapshot

Efficient Determination of the Enantiomeric Purity and Absolute Configuration of Flavanones by Using (S)-3,3′-Dibromo-1,1′-bi-2-naphthol as a Chiral Solvating Agent

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00839openalex-snapshot

Nitric Oxide Inhibitory Activity and Absolute Configurations of Arylalkenyl α,β-Unsaturated δ/γ-Lactones from Cryptocarya concinna

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00986openalex-snapshot

Oxaspirol B with p97 Inhibitory Activity and Other Oxaspirols from Lecythophora sp. FL1375 and FL1031, Endolichenic Fungi Inhabiting Parmotrema tinctorum and Cladonia evansii

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01584openalex-snapshot

Triplinones I–O: Arylalkenyl α,β-Unsaturated-δ-Lactones Isolated from the Leaves of Australian Rainforest Plant Cryptocarya triplinervis (Lauraceae) Displaying Anti-Inflammatory Activity

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00063openalex-snapshot

Structure and Configuration of Phosphoeleganin, a Protein Tyrosine Phosphatase 1B Inhibitor from the Mediterranean Ascidian Sidnyum elegans

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00953openalex-snapshot

Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K–O from Hyptis brevipes

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00133openalex-snapshot

The Berkeleylactones, Antibiotic Macrolides from Fungal Coculture

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00397openalex-snapshot

Assignment of the Absolute Configuration of Phosphoeleganin via Synthesis of Model Compounds

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00457openalex-snapshot

Bioactive Asarone-Derived Phenylpropanoids from the Rhizome of Acorus tatarinowii Schott

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00993openalex-snapshot

Evodialones A and B: Polyprenylated Acylcyclopentanone Racemates with a 3-Ethyl-1,1-diisopentyl-4-methylcyclopentane Skeleton from Evodia lepta

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00713openalex-snapshot

Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricus

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00908openalex-snapshot

Structure Elucidation, Conformation, and Configuration of Cytotoxic 6-Heptyl-5,6-dihydro-2H-pyran-2-ones from Hyptis Species and Their Molecular Docking to α-Tubulin

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00937openalex-snapshot

The Configuration of Distaminolyne A is S: Quantitative Evaluation of Exciton Coupling Circular Dichroism of N,O- Bis-arenoyl-1-amino-2-alkanols

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00578openalex-snapshot

Evidence of Enantiomers of Spiroglycol. Distinction by Using α,α′-Bis(trifluoromethyl)-9,10-anthracenedimethanol as a Chiral Solvating Agent and by Derivatization with Chiral Acids

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01275openalex-snapshot

Using the Competing Enantioselective Conversion Method to Assign the Absolute Configuration of Cyclic Amines with Bode’s Acylation Reagents

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01510openalex-snapshot

The Assignment of the Absolute Configuration of β-Chiral Primary Alcohols with Axially Chiral Trifluoromethylbenzimidazolylbenzoic Acid

inferred← citeshttps://doi.org/10.1021/acs.joc.2c02931openalex-snapshot

Base-Induced Sulfoxide-Sulfenate Rearrangement of 2-Sulfinyl Dienes for the Regio- and Stereoselective Synthesis of Enantioenriched Dienyl Diols

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00706openalex-snapshot

Chiral Recognition Studies of α-(Nonafluoro-tert-butoxy)carboxylic Acids by NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00879openalex-snapshot

Application of 19F NMR Spectroscopy for Determining the Absolute Configuration of α-Chiral Amines and Secondary Alcohols Using Trifluoromethylbenzoimidazolylbenzoic Acid

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01276openalex-snapshot

Development of Ferrocene-Based Diamine-Phosphine-Sulfonamide Ligands for Iridium-Catalyzed Asymmetric Hydrogenation of Ketones

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01749openalex-snapshot

General Quantum-Based NMR Method for the Assignment of Absolute Configuration by Single or Double Derivatization: Scope and Limitations

inferred← citeshttps://doi.org/10.1021/acs.joc.8b02212openalex-snapshot

Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d -Phenylalanine and (1S,2S)-(+)-1,2-Diaminocyclohexane via 1H NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.joc.8b02714openalex-snapshot

Synthesis of (R)- and (S)-Fmoc-Protected Diethylene Glycol Gamma PNA Monomers with High Optical Purity

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00681openalex-snapshot

Synthesis of Structurally Diverse 3-, 4-, 5-, and 6-Membered Heterocycles from Diisopropyl Iminomalonates and SoftC-Nucleophiles

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00884openalex-snapshot

Peyssonnosides A–B, Unusual Diterpene Glycosides with a Sterically Encumbered Cyclopropane Motif: Structure Elucidation Using an Integrated Spectroscopic and Computational Workflow

inferred← citeshttps://doi.org/10.1021/acs.joc.9b01770openalex-snapshot

Axially Chiral Trifluoromethylbenzimidazolylbenzoic Acid: A Chiral Derivatizing Agent for α-Chiral Primary Amines and Secondary Alcohols To Determine the Absolute Configuration

inferred← citeshttps://doi.org/10.1021/acs.joc.9b03129openalex-snapshot

DFT/NMR Approach for the Configuration Assignment of Groups of Stereoisomers by the Combination and Comparison of Experimental and Predicted Sets of Data

inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00706openalex-snapshot

Determination of the Absolute Configuration of CN-Palladacycles by 31P{1H} NMR Spectroscopy Using (1R,2S,5R)-Menthyloxydiphenylphosphine as the Chiral Derivatizing Agent: Efficient Chirality Transfer in Phosphinite Adducts

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02239openalex-snapshot

From Acyclic Intramolecular-[4 + 2]- to Transannular Bis-[4 + 2]-Cycloaddition of the Macrodiolide for the Stereoselective Synthesis of the Octahydronaphthalene Core of Polyenic Macrolactam Sagamilactam

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00030openalex-snapshot

Highly Effective Configurational Assignment Using Bisthioureas as Chiral Solvating Agents in the Presence of DABCO

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01978openalex-snapshot

An Approach for Determining the Absolute Configuration of C-2 in 2-Oxygenated Phenylethanoid Glycosides by 1H NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03855openalex-snapshot

Direct Assignment of the Threo and Erythro Configurations in Polyacetylene Glycosides by 1 H NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03892openalex-snapshot

Asymmetric Total Synthesis of Distaminolyne A and Revision of Its Absolute Configuration

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01189openalex-snapshot

Determination of the Absolute Configuration of β-Chiral Primary Alcohols Using the Competing Enantioselective Conversion Method

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02492openalex-snapshot

Evolvulins I and II, Resin Glycosides with a Trihydroxy Aglycone Unit from Evolvulus alsinoides

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03792openalex-snapshot

One-Pot Absolute Stereochemical Identification of Alcohols via Guanidinium Sulfate Crystallization

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04133openalex-snapshot

Relative and Absolute Structure Assignments of Alkenes Using Crystalline Osmate Derivatives for X-ray Analysis

inferred← citeshttps://doi.org/10.1021/acschembio.3c00452openalex-snapshot

Phosphonate and Thiasugar Analogues of Glucosamine-6-phosphate: Activation of the glmS Riboswitch and Antibiotic Activity

inferred← citeshttps://doi.org/10.1021/acschembio.8b00659openalex-snapshot

Activation of the NLRP3 Inflammasome by Hyaboron, a New Asymmetric Boron-Containing Macrodiolide from the Myxobacterium Hyalangium minutum

inferred← citeshttps://doi.org/10.1021/acsomega.1c01714openalex-snapshot

Cycloartane- and Lanostane-Type Triterpenoids from the Resin of Parthenium argentatum AZ-2, a Byproduct of Guayule Rubber Production

inferred← citeshttps://doi.org/10.1021/acsomega.8b00125openalex-snapshot

Toward the Synthesis of Phormidolides

inferred← citeshttps://doi.org/10.1021/ja061082fopenalex-snapshot

New Chiral Synthons for Efficient Introduction of Bispropionates via Stereospecific Oxonia−Cope Rearrangements

inferred← citeshttps://doi.org/10.1021/ja109226sopenalex-snapshot

Structure and Biosynthesis of the Marine Streptomycete Ansamycin Ansalactam A and Its Distinctive Branched Chain Polyketide Extender Unit

inferred← citeshttps://doi.org/10.1021/ja3104044openalex-snapshot

Thermolides, Potent Nematocidal PKS-NRPS Hybrid Metabolites from Thermophilic Fungus Talaromyces thermophilus

inferred← citeshttps://doi.org/10.1021/jacs.3c03937openalex-snapshot

Optically Enhanced Solid-State 1 H NMR Spectroscopy

inferred← citeshttps://doi.org/10.1021/jacs.5b00556openalex-snapshot

Simultaneous Chirality Sensing of Multiple Amines by 19F NMR

inferred← citeshttps://doi.org/10.1021/jacs.5b09555openalex-snapshot

1H NMR Chiral Analysis of Charged Molecules via Ion Pairing with Aluminum Complexes

inferred← citeshttps://doi.org/10.1021/jm401407wopenalex-snapshot

Stereochemistry of the Tadalafil Diastereoisomers: A Critical Assessment of Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotatory Dispersion

inferred← citeshttps://doi.org/10.1021/jm5008819openalex-snapshot

Synthetic Variants of Mycolactone Bind and Activate Wiskott–Aldrich Syndrome Proteins

inferred← citeshttps://doi.org/10.1021/jo100916xopenalex-snapshot

Development of an Enantioselective Route toward the Lycopodium Alkaloids: Total Synthesis of Lycopodine

inferred← citeshttps://doi.org/10.1021/jo200482dopenalex-snapshot

Synthesis and Characterization of Conformationally Preorganized, (R)-Diethylene Glycol-Containing γ-Peptide Nucleic Acids with Superior Hybridization Properties and Water Solubility

inferred← citeshttps://doi.org/10.1021/jo201450sopenalex-snapshot

Total Synthesis of α-1C-Galactosylceramide, an Immunostimulatory C-Glycosphingolipid, and Confirmation of the Stereochemistry in the First-Generation Synthesis

inferred← citeshttps://doi.org/10.1021/jo301919eopenalex-snapshot

Carbanion-Accelerated Claisen Rearrangements: Asymmetric Induction with Chiral Phosphorus-Stabilized Anions

inferred← citeshttps://doi.org/10.1021/jo400432qopenalex-snapshot

Determination of Absolute Configuration of Secondary Alcohols Using Thin-Layer Chromatography

inferred← citeshttps://doi.org/10.1021/jo401825kopenalex-snapshot

Stereochemistry and Solid-State Structure of an Intrinsically Chiral Meso-Patterned Porphyrin: Case Study by NMR and Single-Crystal X-ray Diffraction Analysis

inferred← citeshttps://doi.org/10.1021/jo8012429openalex-snapshot

A Simple Microscale Method for Determining the Relative Stereochemistry of Statine Units

inferred← citeshttps://doi.org/10.1021/jo802211nopenalex-snapshot

Synthesis of Conformationally Preorganized and Cell-Permeable Guanidine-Based γ-Peptide Nucleic Acids (γGPNAs)

inferred← citeshttps://doi.org/10.1021/jp509988eopenalex-snapshot

Determination of Absolute Configuration in Chiral Solvents with Nuclear Magnetic Resonance. A Combined Molecular Dynamics/Quantum Chemical Study

inferred← citeshttps://doi.org/10.1021/ml500015ropenalex-snapshot

Case Study of Small Molecules As Antimalarials: 2-Amino-1-phenylethanol (APE) Derivatives

inferred← citeshttps://doi.org/10.1021/np100087copenalex-snapshot

Fijiolides A and B, Inhibitors of TNF-α-Induced NFκB Activation, from a Marine-Derived Sediment Bacterium of the Genus Nocardiopsis

inferred← citeshttps://doi.org/10.1021/np100159jopenalex-snapshot

Absolute Configuration of Brevisamide and Brevisin: Confirmation of a Universal Biosynthetic Process for Karenia brevis Polyethers

inferred← citeshttps://doi.org/10.1021/np2000864openalex-snapshot

Smardaesidins A–G, Isopimarane and 20-nor-Isopimarane Diterpenoids from Smardaea sp., a Fungal Endophyte of the Moss Ceratodon purpureus

inferred← citeshttps://doi.org/10.1021/np3005634openalex-snapshot

Plakortolide Stereochemistry Revisited: The Checkered History of Plakortolides E and I

inferred← citeshttps://doi.org/10.1021/np3006088openalex-snapshot

Computationally Assisted Assignment of Kahalalide Y Configuration Using an NMR-Constrained Conformational Search

inferred← citeshttps://doi.org/10.1021/np500233topenalex-snapshot

Bioactive Constituents of Cirsium japonicum var. australe

inferred← citeshttps://doi.org/10.1021/np500840nopenalex-snapshot

Biosynthetic Products from a Nearshore-Derived Gram-Negative Bacterium Enable Reassessment of the Kailuin Depsipeptides

inferred← citeshttps://doi.org/10.1021/np9001724openalex-snapshot

Bioactive 5,6-Dihydro-α-pyrone Derivatives from Hyptis brevipes

inferred← citeshttps://doi.org/10.1021/ol051544eopenalex-snapshot

Synthetic Studies toward Amphidinolide B1: Synthesis of the C9−C26 Fragment

inferred← citeshttps://doi.org/10.1021/ol201902yopenalex-snapshot

Determination of Absolute Configuration Using Kinetic Resolution Catalysts

inferred← citeshttps://doi.org/10.1021/ol402080sopenalex-snapshot

Actinoranone, a Cytotoxic Meroterpenoid of Unprecedented Structure from a Marine Adapted Streptomyces sp.

inferred← citeshttps://doi.org/10.1021/ol500173yopenalex-snapshot

Absolute Configuration Determination Using Enantiomeric Pairs of Molecularly Imprinted Polymers

inferred← citeshttps://doi.org/10.1021/ol701851fopenalex-snapshot

A Catalytic Asymmetric Vinylogous Mukaiyama Aldol Reaction

inferred← citeshttps://doi.org/10.1021/ol900936topenalex-snapshot

A Versatile Route to the Tulearin Class of Macrolactones: Synthesis of a Stereoisomer of Tulearin A

inferred← citeshttps://doi.org/10.1038/s41467-018-04843-zopenalex-snapshot

Assigning the absolute configuration of single aliphatic molecules by visual inspection

inferred← citeshttps://doi.org/10.1038/s41467-019-12453-6openalex-snapshot

Hydrogen-bonded frameworks for molecular structure determination

inferred← citeshttps://doi.org/10.1038/s41598-022-21174-8openalex-snapshot

Application of the 2-deoxyglucose scaffold as a new chiral probe for elucidation of the absolute configuration of secondary alcohols

inferred← citeshttps://doi.org/10.1038/s41598-026-52958-xopenalex-snapshot

Structurally diverse secondary metabolites from the dung-inhabiting fungus Botryotrichum murorum

inferred← citeshttps://doi.org/10.1038/srep29744openalex-snapshot

Involucratusins A–H: Unusual Cadinane Dimers from Stahlianthus involucratus with Multidrug Resistance Reversal Activity

inferred← citeshttps://doi.org/10.1039/b909430jopenalex-snapshot

Luminescent chiral lanthanide(iii) complexes as potential molecular probes

inferred← citeshttps://doi.org/10.1039/c3nj00779kopenalex-snapshot

Ternary ion-pair complexation: a protocol for chiral discrimination and the assignment of absolute configuration of chiral hydroxy acids

inferred← citeshttps://doi.org/10.1039/c3ob42087fopenalex-snapshot

RES-TOCSY: a simple approach to resolve overlapped 1H NMR spectra of enantiomers

inferred← citeshttps://doi.org/10.1039/c4nj00417eopenalex-snapshot

A versatile ternary ionic complex for chiral discrimination of molecules with diverse functionalities using 1 H NMR

inferred← citeshttps://doi.org/10.1039/c5nj01877copenalex-snapshot

Chiral discrimination of β-telluride carboxylic acids by NMR spectroscopy

showing the first 200 of 294

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.