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The Assignment of Absolute Configuration by NMR

https://doi.org/10.1021/cr000665j
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Application of phenylglycine methyl ester (PGME) to determination of the absolute configuration of carboxylic acids having phenylalkyl group
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Novel Acetogenins from the Leaves ofDasymaschalon sootepense
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Modern Methods for the Determination of Optical Purity
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Determination of the Absolute Configuration of Chiral Thiols by 1H‐NMR Spectroscopy of Diastereomeric Thiol Esters
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Absolute Configuration of Bromochlorofluoromethane from Experimental and Ab Initio Theoretical Vibrational Raman Optical Activity
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Chirale Lactole, VI. Eine Methode zur Bestimmung der Absolutkonfiguration chiraler α‐hydroxysubstituierter Nitrile, Alkine und Aldehyde
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Chirale Lactole, VII. O,O‐ und O,N‐Acetalbildungsreaktionen der enantiomerenreinen exo‐anellierten Octahydro‐7,8,8‐trimethyl‐4,7‐methanobenzofuran‐2‐ol‐Schutzgruppe
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Determination of absolute configuration of 1,3‐diols by the modified Mosher's method using their di‐MTPA esters
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Emerging methods for the rapid determination of enantiomeric excess
inferredcites →https://doi.org/10.1002/chir.10145openalex-snapshot
Optical rotation: Recent advances in determining the absolute configuration
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Nonreductive Enantioselective Ring Opening of N‐(Methylsulfonyl)dicarboximides with Diisopropoxytitanium α,α,α′,α′‐Tetraaryl‐1,3‐dioxolane‐4,5‐dimethanolate
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Antarctic Marine Metabolites: New Polyhydroxylated Steroidal Glycosides from the Starfish Odontaster validus
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Antibiotics from Gliding Bacteria, LXXVIII. Ripostatin A, B, and C: Isolation and Structure and Structure Elucidation of Novel Metabolites from Sorangium cellulosum
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inferredcites →https://doi.org/10.1016/0040-4020(76)85011-9openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4020(96)00516-9openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(91)80650-uopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(91)80655-popenalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(92)88083-hopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(94)88034-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(94)88061-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(95)00132-vopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(96)00898-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(96)00954-9openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(96)01368-8openalex-snapshot
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inferredcites →https://doi.org/10.1016/0040-4039(96)01894-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/0079-6565(82)80010-1openalex-snapshot
The determination of absolute configuration using nuclear magnetic resonance techniques
inferredcites →https://doi.org/10.1016/0957-4166(94)00364-hopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0957-4166(95)00241-gopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0957-4166(95)00260-vopenalex-snapshot
1H NMR correlation of chiral 3-phenylbutanoates for the determination of absolute stereochemistry of chiral alcohols
inferredcites →https://doi.org/10.1016/0957-4166(95)00412-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/0957-4166(96)00269-8openalex-snapshot
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inferredcites →https://doi.org/10.1016/b978-0-12-507701-9.50012-7openalex-snapshot
Nuclear Magnetic Resonance Analysis Using Chiral Derivatives
inferredcites →https://doi.org/10.1016/b978-0-12-507701-9.50013-9openalex-snapshot
Nuclear Magnetic Resonance Analysis Using Chiral Solvating Agents
inferredcites →https://doi.org/10.1016/b978-0-12-507701-9.50014-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0021-9673(00)85077-3openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(00)00753-5openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)00056-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)00795-5openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)92244-6openalex-snapshot
Structures of cylindrocyphanes a-f
inferredcites →https://doi.org/10.1016/s0040-4020(01)96470-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(97)00153-1openalex-snapshot
Scanlonenyne, a novel halogenated C 15 acetogenin from the red alga Laurencia obtusa in Irish waters
inferredcites →https://doi.org/10.1016/s0040-4020(97)00291-3openalex-snapshot
The Fucofuranoside Method, a New 1 H and 13 C Nuclear Magnetic Resonance Method to Determine the Absolute Configuration of Secondary Alcohols
inferredcites →https://doi.org/10.1016/s0040-4020(97)00512-7openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(98)00213-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(98)00645-0openalex-snapshot
The fucofuranoside method for determining the absolute configuration of the tertiary alcohols substituted with methyl and two methylene groups
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/s0040-4020(98)83017-2openalex-snapshot
Trifluoromethyl vs. methyl ability to direct enantioselection in microbial reduction of carbonyl substrates.
inferredcites →https://doi.org/10.1016/s0040-4020(99)00332-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(99)00356-7openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(99)00706-1openalex-snapshot
Absolute stereochemistry of cicutoxin and related toxic polyacetylenic alcohols from Cicuta virosa
inferredcites →https://doi.org/10.1016/s0040-4020(99)00932-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)00015-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)00163-5openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)01349-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)01368-xopenalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)01692-0openalex-snapshot
Strongylodiols A, B and C, new cytotoxic acetylenic alcohols isolated from the Okinawan marine sponge of the genus Strongylophora as each enantiomeric mixture with a different ratio
inferredcites →https://doi.org/10.1016/s0040-4039(00)71080-xopenalex-snapshot
The determination of optical purity by nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1016/s0040-4039(00)73366-1openalex-snapshot
New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)75848-5openalex-snapshot
A new method for establishment of absolute configurations of secondary alcohols by NMR spectroscopy
inferredcites →https://doi.org/10.1016/s0040-4039(00)76661-5openalex-snapshot
New chirality recognizing reagents for the determination of absolute stereochemistry and enantiomeric purity by NMR
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(00)78558-3openalex-snapshot
Noe correlations in MTPA, MNCB and MBNC esters
inferredcites →https://doi.org/10.1016/s0040-4039(00)91714-3openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(00)99187-1openalex-snapshot
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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(01)83433-xopenalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(01)92384-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(01)92558-4openalex-snapshot
Use of shift reagent with MTPA derivatives in 1H NMR spectroscopy. II. determination of absolute configuration and diastereomeric composition of secondary carbinols in epimeric mixture
inferredcites →https://doi.org/10.1016/s0040-4039(01)93060-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(01)93127-2openalex-snapshot
Über eine neue methode zur bestimmung der absoluten konfiguration von chiralen sekundären alkoholen und aminen: nmr-spektroskopie von diastereomeren estern und amiden der α-phenylbutter- und hydratropasäure
inferredcites →https://doi.org/10.1016/s0040-4039(01)99251-2openalex-snapshot
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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/s0040-4039(98)00059-8openalex-snapshot
A new approach for the determination of the absolute configuration of secondary alcohols by 1H NMR with O-substituted mandelate derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(98)01286-6openalex-snapshot
A chiral anisotropic reagent for determination of the absolute configuration of a primary amino compound
inferredcites →https://doi.org/10.1016/s0040-4039(98)01800-0openalex-snapshot
Determination of the absolute configuration of linear secondary alcohols adopting one enantiomer of the chiral anisotropic reagents, methoxy-(1-and 2-naphthyl)acetic acids
inferredcites →https://doi.org/10.1016/s0040-4039(99)01291-5openalex-snapshot
Isolation and structures of haterumalides NA, NB, NC, ND, and NE, novel macrolides from an Okinawan Sponge Ircinia sp.
inferredcites →https://doi.org/10.1016/s0040-4039(99)01878-xopenalex-snapshot
Structure and absolute stereochemistry of HIV-1 integrase inhibitor integric acid. A novel eremophilane sesquiterpenoid produced by a Xylaria sp.
inferredcites →https://doi.org/10.1016/s0040-4039(99)01926-7openalex-snapshot
Determination of the absolute configuration of a secondary alcohol by NMR spectroscopy using difluorodinitrobenzene
inferredcites →https://doi.org/10.1016/s0957-4166(00)00053-7openalex-snapshot
2-Methoxy-2-(1-naphthyl)propionic acid, a powerful chiral auxiliary for enantioresolution of alcohols and determination of their absolute configurations by the 1H NMR anisotropy method
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(00)00233-0openalex-snapshot
Absolute configuration of 2-methoxy-2-(2-naphthyl)propionic acid as determined by the 1H NMR anisotropy method
inferredcites →https://doi.org/10.1016/s0957-4166(00)00254-8openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0957-4166(01)00508-0openalex-snapshot
A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR
inferredcites →https://doi.org/10.1016/s0957-4166(02)00242-2openalex-snapshot
Chemo-enzymatic synthesis of enantiomerically pure (R)-2-naphthylmethoxyacetic acid
inferredcites →https://doi.org/10.1016/s0957-4166(02)00268-9openalex-snapshot
Absolute configurations of 2-methoxy-2-(1-naphthyl)propionic acid and 2-methoxy-2-(2-naphthyl)propionic acid as determined by the phenylglycine methyl ester (PGME) method
inferredcites →https://doi.org/10.1016/s0957-4166(02)00510-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0957-4166(97)00081-5openalex-snapshot
The use of ethyl 2-(9-anthryl)-2-hydroxyacetate for assignment of the absolute configuration of carboxylic acids by 1H NMR
inferredcites →https://doi.org/10.1016/s0957-4166(98)00053-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0957-4166(99)00295-5openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0957-4166(99)00451-6openalex-snapshot
Absolute configuration of 2-hydroxy-2-(1-naphthyl)propionic acid as determined by the 1H NMR anisotropy method
inferredcites →https://doi.org/10.1016/s0968-0896(96)00268-4openalex-snapshot
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inferredcites →https://doi.org/10.1021/cr00007a009openalex-snapshot
NMR determination of enantiomeric purity
inferredcites →https://doi.org/10.1021/cr60267a001openalex-snapshot
Nuclear magnetic resonance studies of amides
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/ja00052a018openalex-snapshot
Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives
inferredcites →https://doi.org/10.1021/ja00105a078openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00154a002openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00479a014openalex-snapshot
Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1021/ja00527a600openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00545a049openalex-snapshot
A model for asymmetric induction in the Diels-Alder reaction
inferredcites →https://doi.org/10.1021/ja00545a600openalex-snapshot
Additions and Corrections - Determination of the Absolute Configuration of a Secondary Hydroxy Group in a Chiral Secondary Alcohol Using Glycosidation Shifts in Carbon-13 Nuclear Magnetic Resonance Spectroscopy
inferredcites →https://doi.org/10.1021/ja00718a018openalex-snapshot
Intrinsic and torsional diastereoisomers. The optical purity of (+)-(S)-deoxyephedrine
inferredcites →https://doi.org/10.1021/ja00783a034openalex-snapshot
Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
inferredcites →https://doi.org/10.1021/ja01016a024openalex-snapshot
Nuclear magnetic resonance nonequivalence of diastereomeric esters of .alpha.-substituted phenylacetic acids for the determination of stereochemical purity
inferredcites →https://doi.org/10.1021/ja9620301openalex-snapshot
Kulolide: A Cytotoxic Depsipeptide from a Cephalaspidean Mollusk, Philinopsis speciosa1
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/ja972664nopenalex-snapshot
An NMR Strategy for Determination of Configuration of Remote Stereogenic Centers: 3-Methylcarboxylic Acids
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/ja990597mopenalex-snapshot
Complexation with Barium(II) Allows the Inference of the Absolute Configuration of Primary Amines by NMR
inferredcites →https://doi.org/10.1021/ja992730gopenalex-snapshot
NMR Spectroscopic Determination of the Absolute Configuration of Chiral Sulfoxides via N-(Methoxyphenylacetyl)sulfoximines
inferredcites →https://doi.org/10.1021/jm00263a012openalex-snapshot
New chiral reagent for the determination of enantiomeric purity and absolute configuration of certain substituted .beta.-arylethylamines
inferredcites →https://doi.org/10.1021/jo00003a043openalex-snapshot
Novel marine polyhydroxylated steroids from the starfish Myxoderma platyacanthum
inferredcites →https://doi.org/10.1021/jo00003a067openalex-snapshot
A new aspect of the high-field NMR application of Mosher's method. The absolute configuration of marine triterpene sipholenol A
inferredcites →https://doi.org/10.1021/jo00029a053openalex-snapshot
Elucidation of the relative and absolute stereochemistry of lobatriene, a marine diterpene, by a modified Mosher method
inferredcites →https://doi.org/10.1021/jo00043a018openalex-snapshot
The natural polypropionate-derived esters of the mollusk Onchidium sp
inferredcites →https://doi.org/10.1021/jo00046a009openalex-snapshot
Asymmetric synthesis of tanshindiol A.
inferredcites →https://doi.org/10.1021/jo00052a032openalex-snapshot
Zaragozic acid A, a potent inhibitor of squalene synthase: initial chemistry and absolute stereochemistry
inferredcites →https://doi.org/10.1021/jo00057a017openalex-snapshot
Viridoxins A and B: novel toxins from the fungus Metarhizium flavoviride
inferredcites →https://doi.org/10.1021/jo00057a051openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00059a036openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00070a023openalex-snapshot
Protein tyrosine kinase inhibitory properties of planar polycyclics obtained from the marine sponge Xestospongia cf. carbonaria and from total synthesis
inferredcites →https://doi.org/10.1021/jo00079a026openalex-snapshot
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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
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Synthesis of Dideuterated and Enantiomers of Monodeuterated Tridecanoic Acids at C-9 and C-10 Positions
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Tetra-O-benzoylglucosylation: A New 1H Nuclear Magnetic Resonance Method for Determination of the Absolute Configuration of Secondary Alcohols
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Conformational Structure and Dynamics of Arylmethoxyacetates: DNMR Spectroscopy and Aromatic Shielding Effect
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Determination of the Absolute Stereochemistry of Chiral Amines by 1H NMR of Arylmethoxyacetic Acid Amides: The Conformational Model
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Determination of the absolute configuration of chiral secondary alcohols from tetra-O-acetylglucosidation-induced proton nuclear magnetic resonance shifts
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Novel sponge-derived amino acids. 11. The entire absolute stereochemistry of the bengamides
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On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols
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Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives
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Preparation of (+)-N-methyl-1-(1-naphthyl)ethylamine and the determination of its optical purity by nuclear magnetic resonance
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Nuclear magnetic resonance configuration correlation of primary amine derivatives of .alpha.-methyl-.alpha.-methoxy(pentafluorophenyl)acetic acid
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Absolute Stereochemistry of Amphidinolide E
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Structure and Absolute Stereochemistry of Phormidolide, a New Toxic Metabolite from the Marine Cyanobacterium Phormidium sp.
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Absolute Configuration of Secondary Alcohols by 1H NMR: In Situ Complexation of α-Methoxyphenylacetic Acid Esters with Barium(II)
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Absolute Configuration of tert-Butyl-1-(2-methylnaphthyl)phosphine Oxide
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MTPA (Mosher) Amides of Cyclic Secondary Amines: Conformational Aspects and a Useful Method for Assignment of Amine Configuration
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Applications of MTPA (Mosher) Amides of Secondary Amines: Assignment of Absolute Configuration in Chiral Cyclic Amines
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Determination of the Absolute Configuration of Amines and α-Amino Acids by 1H NMR of (R)-O-Aryllactic Acid Amides
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Absolute Stereochemistry of Soulattrolide and Its Analogues
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Determination of Absolute Configurations of Carbinols of Annonaceous Acetogenins with 2-Naphthylmethoxyacetic Acid Esters
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Oximidines I and II: Novel Antitumor Macrolides from Pseudomonas sp.
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Rubrosides A−H, New Bioactive Tetramic Acid Glycosides from the Marine Sponge Siliquariaspongia japonica1
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Boc-Phenylglycine: The Reagent of Choice for the Assignment of the Absolute Configuration of α-Chiral Primary Amines by 1H NMR Spectroscopy
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Chemical Study and Absolute Configuration of a New Marine Secospatane from the Brown Alga Dilophus okamurae
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Phenylglycine Methyl Ester, a Useful Tool for Absolute Configuration Determination of Various Chiral Carboxylic Acids
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Amphidinolide T, Novel 19-Membered Macrolide from Marine Dinoflagellate Amphidinium sp.
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Assignment of the Absolute Configuration of α-Chiral Carboxylic Acids by 1H NMR Spectroscopy
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Absolute Configuration of a Tetrahydrophenanthrene from Heliotropium ovalifolium by LC-NMR of Its Mosher Esters
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Asimilobin and cis- and trans-Murisolinones, Novel Bioactive Annonaceous Acetogenins from the Seeds of Asimina triloba
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Two Novel Polyhydroxysteroids with a 24-Ethyl-25-hydroxy-26-sulfoxy Side Chain from the Deep Water Starfish Styracaster caroli
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New Type of Mono-tetrahydrofuran Ring Acetogenins from Goniothalamus donnaiensis
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Absolute Configuration of 2,6-Dimethylheptyl Sulfate and Its Distribution in Ascidiacea
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Absolute Configuration of Some Marine Metabolites from Cystoseira spp.
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Bioactive Labdane Diterpenoids from Renealmia alpinia Collected in the Suriname Rainforest
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Three New Metabolites from the Marine Yeast Aureobasidium pullulans
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Cyclic Polyketide Peroxides and Acyclic Diol Analogues from the Sponge Plakortis lita
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Palythoalones A and B, New Ecdysteroids from the Marine Zoanthid Palythoa australiae
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Three Secoiridoid Glucosides from Jasminum nudiflorum
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Tanikolide, a Toxic and Antifungal Lactone from the Marine Cyanobacterium Lyngbya majuscula
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Sesterterpenoids and Diterpenoids of the Wax Excreted by a Scale Insect, Ceroplastes pseudoceriferus
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Thirteen Novel Cycloartane-Type Triterpenes from Combretum quadrangulare
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Chiral Silylation Reagents for the Determination of Absolute Configuration by NMR Spectroscopy
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Absolute Stereochemistry of Amphidinolides G and H
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Absolute Configuration of 1,n-Diols by NMR: The Importance of the Combined Anisotropic Effects in Bis-Arylmethoxyacetates
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“Mix and Shake” Method for Configurational Assignment by NMR: Application to Chiral Amines and Alcohols
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Structure and biosynthesis of kendomycin, a carbocyclic ansa-compound from Streptomyces
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Determination of the absolute configurations of α-amino esters from the 19F NMR chemical shifts of their CFTA amide diastereomers
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Optically active diazacyclophosphamides: novel efficient reagents for the determination of the absolute configuration of amines and alcohols
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Structure elucidation of (22E,24R,25R)-24-methyl-5α-cholest-22-ene-3β,4β,5,6α,8,14,15α,25,26-nonaol and (22E,24S)-24-methyl–5α-cholest-22-ene-3β,4β,5,6α,8,14,15α,25,28-nonaol, minor marine polyhydroxysteroids isolated from the starfish Archaster typicus
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Crystalline State Conformation of 2-Methoxy-2-(1-naphthyl)propionic Acid Ester
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Streptoketol A and B, New Secondary Metabolites with DNA-Binding Properties
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The Biology - Chemistry Interface
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Application of the MTPA Method to Determination of Abusolute Stereochemistry. The Hydroxymethyl-substituted Chiral Carbon of Carbocycles
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Identification of Absolute Configuration of Tertiary Alcohols by Combination of Mosher's Method and Conformational Analysis
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Absolute Configuration of Sipholenol-A. Presence of Two Conformers of MTPA Ester Moiety in a Crystalline State
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Determination of the Absolute Configuration of Ginnol, a Long-chain Aliphatic Alcohol, by Use of a New Chiral Anisotropic Reagent
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Application of Modified Mosher’s Method to α-Aromatic Secondary Alcohols. Exception of the Rule and Conformational Analyses
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Absolute Stereochemistry of Tanabalin, an Insect Antifeedant Clerodane from Tanacetum balsamita
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Determination of Absolute Configurations of Tertiary Alcohols by NMR Spectroscopy
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New derivatization for liquid chromatographic resolution of amino acid enantiomers.
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6S,8R-Stereochemistry of the C27- and C29-Alkane-6,8-diols Isolated from Three Compositae Flowers.
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Identification of the Absolute Configuration of Pectenotoxin-6, a Polyether Macrolide Compound, by NMR Spectroscopic Method Using a Chiral Anisotropic Reagent, Phenylglycine Methyl Ester
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Absolute Configurations of Some Hydroxy-fatty Acids Produced by the Insect Genus Laccifer
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A Cautionary Note on the Use of Commercial (R)-MTPA-Cl and (S)-MTPA-Cl in Determination of Absolute Configuration by Mosher Ester Analysis

What points at this work

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

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inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/chem.200500807openalex-snapshot
Synthesis of Strained Tricyclic β‐Lactams by Intramolecular [2+2] Cycloaddition Reactions of 2‐Azetidinone‐Tethered Enallenols: Control of Regioselectivity by Selective Alkene Substitution
inferred← citeshttps://doi.org/10.1002/chem.200500823openalex-snapshot
Multiple Component Approaches to C‐Glycosyl β‐Amino Acids by Complementary One‐Pot Mannich‐Type and Reformatsky‐Type Reactions
inferred← citeshttps://doi.org/10.1002/chem.200701054openalex-snapshot
Configurational Stability of Oxymethyllithiums as Intermediates in Intramolecular Rearrangements
inferred← citeshttps://doi.org/10.1002/chem.200800475openalex-snapshot
Preparation of α‐Aminobenzylphosphonic Acids with a Stereogenic Quaternary Carbon Atom via Microscopically Configurationally Stable α‐Aminobenzyllithiums
inferred← citeshttps://doi.org/10.1002/chem.200801002openalex-snapshot
Stereoselective Synthesis of Cyclopropanes Based on a 1,2‐Chirality Transfer
inferred← citeshttps://doi.org/10.1002/chem.200801382openalex-snapshot
A Gold‐Catalyzed Entry into the Sesquisabinene and Sesquithujene Families of Terpenoids and Formal Total Syntheses of Cedrene and Cedrol
inferred← citeshttps://doi.org/10.1002/chem.200801478openalex-snapshot
Total Synthesis of Discodermolide: Optimization of the Effective Synthetic Route
inferred← citeshttps://doi.org/10.1002/chem.200801574openalex-snapshot
Noduliprevenone: A Novel Heterodimeric Chromanone with Cancer Chemopreventive Potential
inferred← citeshttps://doi.org/10.1002/chem.200802067openalex-snapshot
Total Syntheses of Amphidinolides B1, B4, G1, H1 and Structure Revision of Amphidinolide H2
inferred← citeshttps://doi.org/10.1002/chem.200901127openalex-snapshot
Bisphosphine‐Functionalized Cyclic Decapeptides Based on the Natural Product Gramicidin S: A Potential Scaffold for Transition‐Metal Coordination
inferred← citeshttps://doi.org/10.1002/chem.200901180openalex-snapshot
Metal‐Catalyzed Cyclization of β‐ and γ‐Allenols Derived from D ‐Glyceraldehyde—Synthesis of Enantiopure Dihydropyrans and Tetrahydrooxepines: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/chem.200901505openalex-snapshot
The Stereochemistry of 1,2,3‐Triols Revealed by 1H NMR Spectroscopy: Principles and Applications
inferred← citeshttps://doi.org/10.1002/chem.200901817openalex-snapshot
Preparation, Modification, and Evaluation of Cruentaren A and Analogues
inferred← citeshttps://doi.org/10.1002/chem.201001520openalex-snapshot
Metal‐Catalyzed Cycloetherification Reactions of β,γ‐ and γ,δ‐Allendiols: Chemo‐, Regio‐, and Stereocontrol in the Synthesis of Oxacycles
inferred← citeshttps://doi.org/10.1002/chem.201003264openalex-snapshot
Concise Synthesis of Complicated Polypropionates through One‐Pot Dissymmetrical Two‐Directional Chain Elongation
inferred← citeshttps://doi.org/10.1002/chem.201100675openalex-snapshot
Conception, Synthesis, and Biological Evaluation of Original Discodermolide Analogues
inferred← citeshttps://doi.org/10.1002/chem.201500050openalex-snapshot
Enantioselective Allylation of (2E,4E)‐2,4‐Dimethylhexadienal: Synthesis of (5R,6S)‐(+)‐Pteroenone
inferred← citeshttps://doi.org/10.1002/chem.201600294openalex-snapshot
Montecrinanes A–C: Triterpenes with an Unprecedented Rearranged Tetracyclic Skeleton from Celastrus vulcanicola. Insights into Triterpenoid Biosynthesis Based on DFT Calculations
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.201900350openalex-snapshot
1,2‐Dihydro‐1‐hydroxy‐2,3,1‐benzodiazaborine Bearing an Acridine Moiety as a Circular Dichroism Probe for Determination of Absolute Configuration of Mono‐Alcohols
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.202002449openalex-snapshot
Syntheses of Thailandepsin B Pseudo‐Natural Products: Access to New Highly Potent HDAC Inhibitors via Late‐Stage Modification
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/chem.202301408openalex-snapshot
Supramolecular Chirogenesis in a Sterically Hindered Porphyrin: A Critical Theoretical Analysis**
inferred← citeshttps://doi.org/10.1002/chem.202402279openalex-snapshot
Investigating the Catalytic Site of Human 15‐Lipoxygenase‐1 via Marine Natural Products
inferred← citeshttps://doi.org/10.1002/chem.71122openalex-snapshot
Chiral Analysis for High‐Throughput Reaction Screening: Recent Advances in Accelerating Asymmetric Catalysis Discovery
inferred← citeshttps://doi.org/10.1002/chin.200414300openalex-snapshot
The Assignment of Absolute Configuration by NMR
inferred← citeshttps://doi.org/10.1002/chir.20074openalex-snapshot
Determination of the absolute configuration of Anisotome irregular diterpenes: Application of CD and NMR methods
inferred← citeshttps://doi.org/10.1002/chir.20076openalex-snapshot
Stereochemical studies of chiral resolving agents, M9PP and H9PP acids
inferred← citeshttps://doi.org/10.1002/chir.20077openalex-snapshot
MαNP acid, a powerful chiral molecular tool for preparation of enantiopure alcohols by resolution and determination of their absolute configurations by the 1H NMR anisotropy method
inferred← citeshttps://doi.org/10.1002/chir.20087openalex-snapshot
Chiral derivatives of 2‐(1‐naphthyl)‐2‐phenylacetic acid
inferred← citeshttps://doi.org/10.1002/chir.20125openalex-snapshot
Assignment of absolute configuration of 3‐hydroxy β‐lactams by the NMR “mix and shake” method
inferred← citeshttps://doi.org/10.1002/chir.20139openalex-snapshot
Application of Mosher's method for absolute configuration assignment and resolution of 2‐hydroxypyrrolizidinones
inferred← citeshttps://doi.org/10.1002/chir.20156openalex-snapshot
Synthesis of enantiopure phthalides including 3‐butylphthalide, a fragrance component of celery oil, and determination of their absolute configurations
inferred← citeshttps://doi.org/10.1002/chir.20176openalex-snapshot
Synthesis of (R)- and (S)-3,3,3-trifluoro-2-phenylpropanoyl isocyanates and their use as reactive analogues of Mosher's acid
inferred← citeshttps://doi.org/10.1002/chir.20236openalex-snapshot
Preparation of enantiopure Wieland–Miescher ketone and derivatives by the MαNP acid method. Substituent effect on the HPLC separation
inferred← citeshttps://doi.org/10.1002/chir.20261openalex-snapshot
Solvent effects on the conformational distribution and optical rotation of γ‐methyl paraconic acids and esters
inferred← citeshttps://doi.org/10.1002/chir.20368openalex-snapshot
Application of chiral technology in a pharmaceutical company. Enantiomeric separation and spectroscopic studies of key asymmetric intermediates using a combination of techniques. Phenylglycidols
inferred← citeshttps://doi.org/10.1002/chir.20385openalex-snapshot
New route to enantiopure MαNP acid, a powerful resolution and chiral 1H NMR anisotropy reagent
inferred← citeshttps://doi.org/10.1002/chir.20399openalex-snapshot
Enantiomeric separation and determination of absolute stereochemistry of asymmetric molecules in drug discovery—Building chiral technology toolboxes
inferred← citeshttps://doi.org/10.1002/chir.20406openalex-snapshot
Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with phosphorylated derivatizing agents from C2‐symmetrical diamines containing the (S)‐α‐phenylethyl group
inferred← citeshttps://doi.org/10.1002/chir.20435openalex-snapshot
Discrimination of enantiomers of α‐amino acids by chiral derivatizing reagents from trans‐1,2‐diaminocyclohexane
inferred← citeshttps://doi.org/10.1002/chir.20441openalex-snapshot
Sugar derived hexacoordinated phosphates: Chiral anionic auxiliaries with general asymmetric efficiency
inferred← citeshttps://doi.org/10.1002/chir.20447openalex-snapshot
The origin of an unusually large 19F chemical shift difference between the diastereomeric α‐cyano‐α‐fluoro‐p‐tolylacetic acid (CFTA) esters of 3′,4′,5,7‐tetra‐O‐methylepicatechin
inferred← citeshttps://doi.org/10.1002/chir.20449openalex-snapshot
Chiral NMR discrimination of amines: Analysis of secondary, tertiary, and prochiral amines using (18‐crown‐6)‐2,3,11,12‐tetracarboxylic acid
inferred← citeshttps://doi.org/10.1002/chir.20478openalex-snapshot
Determination of absolute configurations by X‐ray crystallography and 1H NMR anisotropy
inferred← citeshttps://doi.org/10.1002/chir.20518openalex-snapshot
HPLC enantioseparation and absolute configuration of novel anti‐inflammatory pyrrole derivatives
inferred← citeshttps://doi.org/10.1002/chir.20524openalex-snapshot
Determination of absolute configuration—An overview related to this Special Issue
inferred← citeshttps://doi.org/10.1002/chir.20605openalex-snapshot
Chiral recognition of ethers by NMR spectroscopy
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.20654openalex-snapshot
Chiral HPLC separation and absolute configuration of novel S‐DABO derivatives
inferred← citeshttps://doi.org/10.1002/chir.20687openalex-snapshot
NMR enantiodifferentiation of quaternary ammonium salts of Tröger base
inferred← citeshttps://doi.org/10.1002/chir.20786openalex-snapshot
Molecular tweezers for enantiodiscrimination in NMR: Di‐(R,R)‐1‐[10‐(1‐hydroxy‐2,2,2‐trifluoroethyl)‐9‐anthryl]‐2,2,2‐trifluoroethyl benzenedicarboxylates
inferred← citeshttps://doi.org/10.1002/chir.20795openalex-snapshot
Absolute structural elucidation of natural products—A focus on quantum‐mechanical calculations of solid‐state CD spectra
inferred← citeshttps://doi.org/10.1002/chir.20889openalex-snapshot
Assignment of absolute configuration using chiral reagents and NMR spectroscopy
inferred← citeshttps://doi.org/10.1002/chir.20948openalex-snapshot
Application of L ‐proline derivatives as chiral shift reagents for enantiomeric recognition of carboxylic acids
inferred← citeshttps://doi.org/10.1002/chir.20994openalex-snapshot
Enantiopure Ti(IV) amino triphenolate complexes as NMR chiral solvating agents
inferred← citeshttps://doi.org/10.1002/chir.21989openalex-snapshot
First isolation of disubstituted cis‐5,6‐dihydro‐1,10‐phenanthrolines. lipase‐mediated resolution of cis‐ and trans‐phenoxy alcohol isomers and assignment of absolute stereochemistry via cd and nmr spectroscopy
inferred← citeshttps://doi.org/10.1002/chir.22002openalex-snapshot
Evaluation of (R)‐(−)‐α‐methoxy phenyl acetic acid as a chiral shift reagent for resolution and determination of R and S enantiomers of modafinil in bulk drugs and formulations by 1H NMR spectroscopy
inferred← citeshttps://doi.org/10.1002/chir.22114openalex-snapshot
Enantiomeric Discrimination of Isoxazoline Fused β‐amino Acid Derivatives using (18‐Crown‐6)‐2,3,11,12‐tetracarboxylic Acid as a Chiral NMR Solvating Agent
inferred← citeshttps://doi.org/10.1002/chir.22217openalex-snapshot
Synthesis and Quantitative Analysis of Diastereomeric Linked Ester Conjugates With Remote Stereocenters Using High‐Field NMR and Chiral HPLC
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.22395openalex-snapshot
Determination of the Absolute Configuration of Two Pairs of C‐8 − C‐9′ Linked Neolignan Enantiomers
inferred← citeshttps://doi.org/10.1002/chir.22748openalex-snapshot
Chiral Molecular Science: How were the absolute configurations of chiral molecules determined? “Experimental results and theories”
inferred← citeshttps://doi.org/10.1002/chir.22775openalex-snapshot
Di(1‐naphthyl) methanol ester of carboxylic acids for absolute stereochemical determination
inferred← citeshttps://doi.org/10.1002/chir.22854openalex-snapshot
Amino acids as chiral derivatizing agents for antiproliferative substituted N‐benzyl isoindolinones
inferred← citeshttps://doi.org/10.1002/chir.22855openalex-snapshot
Enantioselective complexation of 1‐phenylethanol with chiral compounds bearing urea moiety
inferred← citeshttps://doi.org/10.1002/chir.23030openalex-snapshot
NMR chiral discrimination of chalcogen containing secondary alcohols
inferred← citeshttps://doi.org/10.1002/chir.23057openalex-snapshot
Green synthesis of enantiopure quinoxaline alcohols using Daucus carota
inferred← citeshttps://doi.org/10.1002/chir.23336openalex-snapshot
Nuclear magnetic resonance chiral discrimination of fipronil and malathion agrochemicals: A case study
inferred← citeshttps://doi.org/10.1002/chir.23347openalex-snapshot
Enantiopure cryptophane derivatives: Synthesis and chiroptical properties
inferred← citeshttps://doi.org/10.1002/chir.23406openalex-snapshot
Chiral 2‐phenyl‐3‐hydroxypropyl esters as PKC‐alpha modulators: HPLC enantioseparation, NMR absolute configuration assignment, and molecular docking studies
inferred← citeshttps://doi.org/10.1002/chir.23668openalex-snapshot
Enantioselective high‐performance liquid chromatography combined with spectroscopic methods and theoretical calculations: A valid strategy to determine the absolute configuration of eugenol derivatives
inferred← citeshttps://doi.org/10.1002/chir.70127openalex-snapshot
Diastereotopic Fluorines of CF 2 Group as Stereochemical Probes for Empirical 19 F NMR‐Based Assignment of Absolute Configuration of an Epimeric Center. 21,21‐Difluorothevinols
inferred← citeshttps://doi.org/10.1002/chir.70129openalex-snapshot
Absolute Configuration Assignment From a Single Reflection Using Resonant X‐Ray Diffraction
inferred← citeshttps://doi.org/10.1002/cjoc.202100564openalex-snapshot
Xishaglaucumins A—J, New Cembranoids with Anti‐Inflammatory Activities from the South China Sea Soft Coral Sarcophyton glaucum
inferred← citeshttps://doi.org/10.1002/cmr.a.20110openalex-snapshot
NMR studies of chiral organic compounds in non‐isotropic phases
inferred← citeshttps://doi.org/10.1002/cphc.201301130openalex-snapshot
Enantiodifferentiation through Frequency‐Selective Pure‐Shift 1H Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1002/cphc.202400104openalex-snapshot
Controlling Chirogenic Effects in Porphyrin Based Supramolecular Systems: Theoretical Analysis Versus Experimental Observations
inferred← citeshttps://doi.org/10.1002/cplu.202300080openalex-snapshot
Dynamic Covalent Reactions and Chirality Sensing with Diphenylethene Derived Hemiaminals
inferred← citeshttps://doi.org/10.1002/ejoc.200400870openalex-snapshot
Fulicineroside, an Unusual Glycosidic Dibenzofuran Metabolite from the Slime Mold Fuligo cinerea (Schwein.) Morgan
inferred← citeshttps://doi.org/10.1002/ejoc.200500991openalex-snapshot
A Two‐Step Chemoenzymatic Synthesis of the Natural Pheromone (+)‐Sitophilure Utilizing Isolated, NADPH‐Dependent Ketoreductases
inferred← citeshttps://doi.org/10.1002/ejoc.200600856openalex-snapshot
Conformational Analysis of MαNP Esters, Powerful Chiral Resolution and 1 H NMR Anisotropy Tools – Aromatic Geometry and Solvent Effects on Δ δ Values
inferred← citeshttps://doi.org/10.1002/ejoc.200700490openalex-snapshot
Cyclic Allyl Carbamates in Stereoselective syn SE′ Processes: Synthetic Approach to Sarcodictyins and Eleutherobin
inferred← citeshttps://doi.org/10.1002/ejoc.200700966openalex-snapshot
Structural Elucidation with NMR Spectroscopy: Practical Strategies for Organic Chemists
inferred← citeshttps://doi.org/10.1002/ejoc.200900089openalex-snapshot
An Unusual Conformation of α‐Haloamides Due to Cooperative Binding with Zincated Porphyrins
inferred← citeshttps://doi.org/10.1002/ejoc.200901255openalex-snapshot
Quantum Mechanical Calculation of NMR Parameters in the Stereostructural Determination of Natural Products
inferred← citeshttps://doi.org/10.1002/ejoc.201000712openalex-snapshot
Enantiomerically Pure and Highly Substituted Alicyclic α,α‐Difluoro Ketones: Potential Inhibitors for Malarial Aspartic Proteases, the Plasmepsins
inferred← citeshttps://doi.org/10.1002/ejoc.201001107openalex-snapshot
The Use of a Single Derivative in the Configurational Assignment of Ketone Cyanohydrins
inferred← citeshttps://doi.org/10.1002/ejoc.201001315openalex-snapshot
Total Syntheses of Rhodiolosides A and D and of Sachalinols A–C
inferred← citeshttps://doi.org/10.1002/ejoc.201100003openalex-snapshot
Stereoselective Synthesis and Biological Evaluation of Ferrocene‐Containing 5‐Hydroxyeicosatetraenoic Acid Analogues
inferred← citeshttps://doi.org/10.1002/ejoc.201100209openalex-snapshot
N‐Arylcarbonylpseudoprolines as Tunable Chiral Derivatizing Agents for the Determination of the Absolute Configuration of Secondary Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201100368openalex-snapshot
Enzymatic Total Synthesis of Banana Volatile (S)‐2‐Pentyl (R)‐3‐Hydroxyhexanoate
inferred← citeshttps://doi.org/10.1002/ejoc.201101525openalex-snapshot
Recent Advances in the Total Synthesis of Chlorosulfolipids
inferred← citeshttps://doi.org/10.1002/ejoc.201101728openalex-snapshot
A Concise Total Synthesis of the Non‐peptide Bradykinin B1 Receptor Antagonist Velutinol A
inferred← citeshttps://doi.org/10.1002/ejoc.201200533openalex-snapshot
Structures and Antibacterial Activities of Minor Dolabellanes from the Brown Alga Dilophus spiralis
inferred← citeshttps://doi.org/10.1002/ejoc.201201247openalex-snapshot
Total Synthesis of Eupomatilones 1, 2, and 5 by Enantioselective [2,3]‐Wittig Rearrangement
inferred← citeshttps://doi.org/10.1002/ejoc.201300055openalex-snapshot
Synthesis and Structural Studies of α/β‐Peptides Derived from Fused Furano‐pyran β‐Amino Acid and L‐Ala
inferred← citeshttps://doi.org/10.1002/ejoc.201300439openalex-snapshot
On the Configurational Stability of Chiral Heteroatom‐Substituted [D1]Methylpalladium Complexes as Intermediates of Stille and Suzuki–Miyaura Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201301445openalex-snapshot
Sesquiterpenes from Artemisia argyi: Absolute Configurations and Biological Activities
inferred← citeshttps://doi.org/10.1002/ejoc.201402123openalex-snapshot
Design and Study of Peptides Containing 1:1 Left‐ and Right‐Handed Helical Patterns from Aminopyrancarboxylic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201402987openalex-snapshot
Addition of Vinylmetallic Reagents to Chiral 2‐Formyltetrahydrofuran
inferred← citeshttps://doi.org/10.1002/ejoc.201403094openalex-snapshot
Enantioselective Allylation of tert‐Butyldimethylsilyl‐Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana
inferred← citeshttps://doi.org/10.1002/ejoc.201600399openalex-snapshot
Enantioselective Catalysis by Chiral Isothioureas
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.201800219openalex-snapshot
Total Synthesis of Catunaregin and Preliminary Evaluation of Its Antitumor Activity
inferred← citeshttps://doi.org/10.1002/ejoc.201800689openalex-snapshot
An Improved Synthesis of the Antibiotic Dehydrophos
inferred← citeshttps://doi.org/10.1002/ejoc.201901878openalex-snapshot
Elucidating the Relative and Absolute Configuration of Organic Compounds by Quantum Mechanical Approaches
inferred← citeshttps://doi.org/10.1002/ejoc.202000711openalex-snapshot
Determination of the Absolute Configurations of Chiral Alkanes – An Analysis of the Available Tools
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/ejoc.202200410openalex-snapshot
Asymmetric Reduction of α,α‐Dichloro‐β‐Keto Esters by NADPH‐Dependent Ketoreductases
inferred← citeshttps://doi.org/10.1002/ejoc.202200636openalex-snapshot
Organocatalytic Synthesis and Anti‐Trypanosomal Activity Evaluation of L‐Pentofuranose‐Mimetic Iminosugars
inferred← citeshttps://doi.org/10.1002/ejoc.202201329openalex-snapshot
Stereoselective Synthesis of γ‐(Acyloxy)carboxylic Acids and γ‐Lactones Featuring the Switch of Stereopreference of Candida antarctica Lipase B in Sodium γ‐Hydroxycarboxylate Homologues
inferred← citeshttps://doi.org/10.1002/hlca.202000081openalex-snapshot
Chiral α‐Amino Acid‐Based NMR Solvating Agents
inferred← citeshttps://doi.org/10.1002/ijch.202000004openalex-snapshot
Merging Macromolecular and Supramolecular Chemistry into Bioinspired Synthesis of Complex Systems
inferred← citeshttps://doi.org/10.1002/ijch.202000103openalex-snapshot
Beyond Allylic Alkylation: Applications of Trost Chemistry in Complex Molecule Synthesis
inferred← citeshttps://doi.org/10.1002/ijch.202100057openalex-snapshot
Helical Chirality of Supramolecular Columns and Spheres Self‐Organizes Complex Liquid Crystals, Crystals, and Quasicrystals
inferred← citeshttps://doi.org/10.1002/mrc.1531openalex-snapshot
Total structural assignment and absolute configuration of terreinol by 13C and 1H NMR
inferred← citeshttps://doi.org/10.1002/mrc.1716openalex-snapshot
Assignment of absolute configuration of cyclic secondary amines by NMR techniques using Mosher's method: a general procedure exemplified with (−)‐isoanabasine
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/mrc.2768openalex-snapshot
Complete 1H and 13C NMR data assignment of protolimonoids from the stem barks of Aphanamixis grandifolia
inferred← citeshttps://doi.org/10.1002/mrc.2855openalex-snapshot
Chiral discrimination of aliphatic amines and amino alcohols using NMR spectroscopy
inferred← citeshttps://doi.org/10.1002/mrc.3886openalex-snapshot
Chiral discrimination of amines by anisotropic NMR parameters using chiral polyacrylamide‐based gels
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.4222openalex-snapshot
Differentiation of enantiomers by 2D NMR spectroscopy at 1 T using residual dipolar couplings
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