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Phenylglycine Methyl Ester, a Useful Tool for Absolute Configuration Determination of Various Chiral Carboxylic Acids

https://doi.org/10.1021/jo991218a
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What this work says

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

inferredcites →https://doi.org/10.1016/0040-4020(96)00516-9openalex-snapshot
The application of 1H nuclear magnetic resonance spectroscopy for the determination of the absolute configuration of chiral carboxylic acids
inferredcites →https://doi.org/10.1016/0040-4039(95)00132-vopenalex-snapshot
New chiral anisotropic reagents for determining the absolute configuration of carboxylic acids
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/s0040-4039(00)96213-0openalex-snapshot
Asymmetric bromolactonization reaction: Synthesis of optically active 2-hydroxy-2-methylalkanoic acids from 2-methylenealkanoic acids
inferredcites →https://doi.org/10.1016/s0040-4039(01)81294-6openalex-snapshot
Photoreduction of 2,4,6-triisopropylbenzophenones with s-butylamine
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/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/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/ja972550bopenalex-snapshot
Assignment of the Absolute Configuration of β-Chiral Primary Alcohols by NMR: Scope and Limitations
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/jo00952a006openalex-snapshot
Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives
inferredcites →https://doi.org/10.1248/cpb.47.684openalex-snapshot
A Convenient One-Pot Synthesis of Quaternary .ALPHA.-Methoxy- and .ALPHA.-Hydroxycarboxylic Acids.
inferredcites →https://doi.org/10.1271/bbb.61.1783openalex-snapshot
Identification of the Absolute Configuration of Pectenotoxin-6, a Polyether Macrolide Compound, by NMR Spectroscopic Method Using a Chiral Anisotropic Reagent, Phenylglycine Methyl Ester

What points at this work

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

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(1H-Benzotriazol-1-yloxy)tripyrrolidino-phosphonium Hexafluorophosphate
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Determination of Enantiomeric Purity and Absolute Configuration by NMR Spectroscopy
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Ulleungamides A and B, Modified α,β-Dehydropipecolic Acid Containing Cyclic Depsipeptides from Streptomyces sp. KCB13F003
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Bombyxamycins A and B, Cytotoxic Macrocyclic Lactams from an Intestinal Bacterium of the Silkworm Bombyx mori
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Polycyclic Macrolactams Generated via Intramolecular Diels–Alder Reactions from an Antarctic Streptomyces Species
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The Assignment of Absolute Configuration by NMR
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Unusual Effects in the Pd-Catalyzed Asymmetric Allylic Alkylations: Synthesis of Chiral Chromans
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Biomimetic Enantioselective Total Synthesis of (−)-Siccanin via the Pd-Catalyzed Asymmetric Allylic Alkylation (AAA) and Sequential Radical Cyclizations
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Flexible Biphenyl Chromophore as a Circular Dichroism Probe for Assignment of the Absolute Configuration of Carboxylic Acids
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Total Synthesis and Complete Structural Assignment of Yaku’amide A
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Asymmetric Induction via Short-Lived Chiral Enolates with a Chiral C–O Axis
inferred← citeshttps://doi.org/10.1021/jacs.6c11673openalex-snapshot
Canalesolide A, a Structurally Unique Polyhydroxy Macrolide from the Marine Cyanobacterium Okeania sp. with Potent Antitrypanosomal Activity
inferred← citeshttps://doi.org/10.1021/jacs.7b02432openalex-snapshot
Collaborative Biosynthesis of Maleimide- and Succinimide-Containing Natural Products by Fungal Polyketide Megasynthases
inferred← citeshttps://doi.org/10.1021/jm400542hopenalex-snapshot
Investigation of the Noncovalent Binding Mode of Covalent Proteasome Inhibitors around the Transition State by Combined Use of Cyclopropylic Strain-Based Conformational Restriction and Computational Modeling
inferred← citeshttps://doi.org/10.1021/jm901848bopenalex-snapshot
Investigation of the Bioactive Conformation of Histamine H3 Receptor Antagonists by the Cyclopropylic Strain-Based Conformational Restriction Strategy
inferred← citeshttps://doi.org/10.1021/jo0011437openalex-snapshot
Total Synthesis of (−)-Heliannuol E
inferred← citeshttps://doi.org/10.1021/jo010752ropenalex-snapshot
Intramolecularly Competitive Ireland-Claisen Rearrangements: Scope and Potential Applications to Natural Product Synthesis
inferred← citeshttps://doi.org/10.1021/jo0492923openalex-snapshot
Asymmetric Intramolecular Michael Addition of α-Sulfinyl Vinylic Carbanion to Enoates
inferred← citeshttps://doi.org/10.1021/jo060958yopenalex-snapshot
Cytotoxic Macrolides from a New Species of the Deep-Water Marine Sponge Leiodermatium
inferred← citeshttps://doi.org/10.1021/jo401974gopenalex-snapshot
Ohmyungsamycins A and B: Cytotoxic and Antimicrobial Cyclic Peptides Produced by Streptomyces sp. from a Volcanic Island
inferred← citeshttps://doi.org/10.1021/jo701544kopenalex-snapshot
Quesnoin, a Novel Pentacyclic ent-Diterpene from 55 Million Years Old Oise Amber
inferred← citeshttps://doi.org/10.1021/np000135iopenalex-snapshot
Novel Norsesquiterpenoids from the Roots of Phyllanthus emblica
inferred← citeshttps://doi.org/10.1021/np010059zopenalex-snapshot
Novel Sesquiterpenoids from the Roots of Phyllanthus emblica
inferred← citeshttps://doi.org/10.1021/np0103261openalex-snapshot
Isolation and Absolute Configuration of ent-Halimane Diterpenoids from Hymenaea courbaril from the Suriname Rain Forest
inferred← citeshttps://doi.org/10.1021/np020097yopenalex-snapshot
Biologically Active Polyketide Metabolites from an Undetermined Fungicolous Hyphomycete Resembling Cladosporium
inferred← citeshttps://doi.org/10.1021/np020440zopenalex-snapshot
New Acetylenic Acids from the Marine Sponge Stelletta Species
inferred← citeshttps://doi.org/10.1021/np030268eopenalex-snapshot
New Cytotoxic Sesterterpenoids and Norsesterterpenoids from Two Sponges of the Genus Sarcotragus
inferred← citeshttps://doi.org/10.1021/np060327zopenalex-snapshot
Penifulvins B−E and a Silphinene Analogue: Sesquiterpenoids from a Fungicolous Isolate of Penicillium griseofulvum
inferred← citeshttps://doi.org/10.1021/np0780147openalex-snapshot
Sesterterpenoids from the Sponge Sarcotragus sp.
inferred← citeshttps://doi.org/10.1021/np100646nopenalex-snapshot
Sesquiterpenes from Blumea balsamifera
inferred← citeshttps://doi.org/10.1021/np200076topenalex-snapshot
Veraguamides A−G, Cyclic Hexadepsipeptides from a Dolastatin 16-Producing Cyanobacterium Symploca cf. hydnoides from Guam
inferred← citeshttps://doi.org/10.1021/np200742copenalex-snapshot
Jomthonic Acid A, a Modified Amino Acid from a Soil-Derived Streptomyces
inferred← citeshttps://doi.org/10.1021/np401071xopenalex-snapshot
Campechic Acids A and B: Anti-invasive Polyether Polyketides from a Soil-Derived Streptomyces
inferred← citeshttps://doi.org/10.1021/np500156nopenalex-snapshot
Suvanine Sesterterpenes and Deacyl Irciniasulfonic Acids from a Tropical Coscinoderma sp. Sponge
inferred← citeshttps://doi.org/10.1021/np500753qopenalex-snapshot
Additional Sesterterpenes and a Nortriterpene Saponin from the Sponge Clathria gombawuiensis
inferred← citeshttps://doi.org/10.1021/ol006697aopenalex-snapshot
Highly Stereoselective Intramolecular Michael Addition Using α-Sulfinyl Vinyllithium as an Unprecedented Michael Donor
inferred← citeshttps://doi.org/10.1021/ol202944gopenalex-snapshot
Erythrazoles A–B, Cytotoxic Benzothiazoles from a Marine-DerivedErythrobactersp.
inferred← citeshttps://doi.org/10.1021/ol300108zopenalex-snapshot
Tripartilactam, a Cyclobutane-Bearing Tricyclic Lactam from a Streptomyces sp. in a Dung Beetle’s Brood Ball
inferred← citeshttps://doi.org/10.1021/ol400687bopenalex-snapshot
Hyrtimomines A–C, New Heteroaromatic Alkaloids from a Sponge Hyrtios sp.
inferred← citeshttps://doi.org/10.1021/ol400781bopenalex-snapshot
Benzophenones from an Endophytic Fungus, Graphiopsis chlorocephala , from Paeonia lactiflora Cultivated in the Presence of an NAD + -Dependent HDAC Inhibitor
inferred← citeshttps://doi.org/10.1021/ol502528mopenalex-snapshot
Agelamadins C–E, Bromopyrrole Alkaloids Comprising Oroidin and 3-Hydroxykynurenine from a Marine Sponge Agelas sp.
inferred← citeshttps://doi.org/10.1021/ol8028719openalex-snapshot
New Chiral Derivatizing Agents: Convenient Determination of Absolute Configurations of Free Amino Acids by 1H NMR
inferred← citeshttps://doi.org/10.1021/op700181nopenalex-snapshot
First Scale-Up: Problems and Resolutions on the Synthesis of WAY-253752, a Novel, Dual-Acting SSRI/5HT1A Antagonist
inferred← citeshttps://doi.org/10.1038/ja.2015.45openalex-snapshot
Cinatrins D and E, and virgaricin B, three novel compounds produced by a fungus, Virgaria boninensis FKI-4958
inferred← citeshttps://doi.org/10.1038/ja.2015.85openalex-snapshot
Isolation and structure elucidation of new phthalide and phthalane derivatives, isolated as antimicrobial agents from Emericella sp. IFM57991
inferred← citeshttps://doi.org/10.1038/s41429-023-00644-9openalex-snapshot
Iseoic acids and bisiseoate: three new naphthohydroquinone/naphthoquinone-class metabolites from a coral-derived Streptomyces
inferred← citeshttps://doi.org/10.1039/b506375bopenalex-snapshot
Diastereoselective Ni(0)-catalyzed carbocyclization to chiral vinylic sulfoxide
inferred← citeshttps://doi.org/10.1039/b926356jopenalex-snapshot
Crystal conformations and molecular packing of (S)-2-methoxy-2-(9-phenanthryl)propanoic acid and a diastereomeric amide prepared from (R)-2-methoxy-2-(1-naphthyl)propanoic acid
inferred← citeshttps://doi.org/10.1039/c2ob26168eopenalex-snapshot
Aminoindanol-based chiral derivatizing agents for the determination of the absolute configuration of carboxylic acids
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/c5ra06959aopenalex-snapshot
Modified Kagan's amide: synthesis and application as a chiral solvating agent for hydrogen-bonding based chiral discrimination in NMR
inferred← citeshttps://doi.org/10.1039/c5ra11919gopenalex-snapshot
A simple and rapid approach for testing enantiopurity of hydroxy acids and their derivatives using 1 H NMR spectroscopy
inferred← citeshttps://doi.org/10.1039/c6ob01234eopenalex-snapshot
Enantioselective synthesis of β-amino acid derivatives via nickel-promoted regioselective carboxylation of ynamides and rhodium-catalyzed asymmetric hydrogenation
inferred← citeshttps://doi.org/10.1039/c8ob01068dopenalex-snapshot
Auto-oxidation promoted sp 3 C–H arylation of glycine derivatives
inferred← citeshttps://doi.org/10.1039/c9np00069kopenalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1039/d2np00064dopenalex-snapshot
Organic synthesis in the study of terpene-derived oxidation products in the atmosphere
inferred← citeshttps://doi.org/10.1039/d2ob01715fopenalex-snapshot
Helix-forming aliphatic homo-δ-peptide foldamers based on the conformational restriction effects of cyclopropane
inferred← citeshttps://doi.org/10.1039/d2ob02286aopenalex-snapshot
Hakuhybotrol, a polyketide produced by Hypomyces pseudocorticiicola , characterized with the assistance of 3D ED/MicroED
inferred← citeshttps://doi.org/10.1039/d4np00061gopenalex-snapshot
Configurational assignments of type-I polyketide synthase (PKS)-derived natural products based on spectroscopic and chemical analysis: methodologies and case studies
inferred← citeshttps://doi.org/10.1039/d4ob01642dopenalex-snapshot
Highly oxygenated steroids with immunosuppressive activity from Solanum undatum
inferred← citeshttps://doi.org/10.1039/d5nj03288aopenalex-snapshot
Enantiodifferentiation of chiral hydroxy acids via 19 F NMR
inferred← citeshttps://doi.org/10.1039/np9900700269openalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1071/ch12179openalex-snapshot
The Synthesis of a Cubane-Substituted Dipeptide
inferred← citeshttps://doi.org/10.1073/pnas.1716245115openalex-snapshot
Discovery of the leinamycin family of natural products by mining actinobacterial genomes
inferred← citeshttps://doi.org/10.1073/pnas.2424388122openalex-snapshot
Identification of the lydiamycin biosynthetic gene cluster in a plant pathogen guides structural revision and identification of molecular target
inferred← citeshttps://doi.org/10.1093/bbb/zbaa086openalex-snapshot
Unexpected reversal of stereochemistry observed in the addition of methallyltrimethylsilane to a chiral α-keto imide
inferred← citeshttps://doi.org/10.1101/2024.11.13.623425openalex-snapshot
Discovery of lydiamycin A biosynthetic gene cluster in the plant pathogen Rhodococcus fascians guides structural revision and identification of molecular target
inferred← citeshttps://doi.org/10.1139/cjc-2021-0163openalex-snapshot
NMR and X-ray studies of apetalic acid isolated from Calophyllum brasiliense and of its chiral amides
inferred← citeshttps://doi.org/10.1177/1934578x1200700707openalex-snapshot
Distinguishing between R - and S -Antcin C and Their Cytotoxicity
inferred← citeshttps://doi.org/10.1246/bcsj.20160224openalex-snapshot
Exploiting Ruthenium Carbene-Catalyzed Reactions in Total Synthesis of Marine Oxacyclic Natural Products
inferred← citeshttps://doi.org/10.1246/bcsj.75.2337openalex-snapshot
Bioorganic Studies on Nyctinasty of the Plant Controlled by a Biological Clock
inferred← citeshttps://doi.org/10.1246/bcsj.79.965openalex-snapshot
The Modified Mosher’s Method and the Sulfoximine Method
inferred← citeshttps://doi.org/10.1246/cl.2002.1118openalex-snapshot
Visualization of the Precise Structure Recognition of Leaf-opening Substance by Using Biologically Inactive Probe Compounds: Fluorescence Studies of Nyctinasty in Legumes 2
inferred← citeshttps://doi.org/10.1248/cpb.59.88openalex-snapshot
Hyaluronidase Inhibitory Rosmarinic Acid Derivatives from Meehania urticifolia
inferred← citeshttps://doi.org/10.1248/cpb.60.121openalex-snapshot
Hyaluronidase Inhibitors from Keiskea japonica
inferred← citeshttps://doi.org/10.1248/cpb.c16-00245openalex-snapshot
Bromopyrrole Alkaloids from Okinawan Marine Sponges Agelas spp.
inferred← citeshttps://doi.org/10.1248/cpb.c18-00072openalex-snapshot
Diastereoselective Total Synthesis and Structural Confirmation of Surugamide F
inferred← citeshttps://doi.org/10.1271/bbb.70266openalex-snapshot
A Tyrosinase Inhibitor, Daedalin A, from Mycelial Culture ofDaedalea dickinsii
inferred← citeshttps://doi.org/10.2323/jgam.2022.03.001openalex-snapshot
17T223A, a new spiroximicin family compound from Streptomyces sp.
inferred← citeshttps://doi.org/10.26434/chemrxiv-2021-k0hj9openalex-snapshot
Design, synthesis, and structural characterization of helix-forming aliphatic homo-δ-peptides based on conformational restriction due to the structural characteristics of cyclopropane
inferred← citeshttps://doi.org/10.26434/chemrxiv.13475928openalex-snapshot
Total Synthesis of the Alleged Structure of Crenarchaeol Enables Structure Revision
inferred← citeshttps://doi.org/10.3109/14756366.2014.961447openalex-snapshot
Chiral resolution, determination of absolute configuration, and biological evaluation of (1,2-benzothiazin-4-yl)acetic acid enantiomers as aldose reductase inhibitors
inferred← citeshttps://doi.org/10.3389/fchem.2019.00318openalex-snapshot
Assigning the Absolute Configurations of Chiral Primary Amines Based on Experimental and DFT-Calculated 19F Nuclear Magnetic Resonance
inferred← citeshttps://doi.org/10.3390/md11010136openalex-snapshot
Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
inferred← citeshttps://doi.org/10.3390/md17070423openalex-snapshot
Cytotoxic Sesquiterpenoid Quinones and Quinols, and an 11-Membered Heterocycle, Kauamide, from the Hawaiian Marine Sponge Dactylospongia elegans
inferred← citeshttps://doi.org/10.3390/md19080413openalex-snapshot
Ochraceopetalin, a Mixed-Biogenetic Salt of Polyketide and Amino Acid Origins from a Marine-Derived Aspergillus ochraceopetaliformis Fungus
inferred← citeshttps://doi.org/10.3390/md19090514openalex-snapshot
Marine Pyrrole Alkaloids
inferred← citeshttps://doi.org/10.3390/md22120524openalex-snapshot
Structural Elucidation and Antiviral Properties of Pannosides from the Halophyte Aster tripolium L.
inferred← citeshttps://doi.org/10.3390/molecules23061336openalex-snapshot
Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
inferred← citeshttps://doi.org/10.3390/ph15121520openalex-snapshot
Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
inferred← citeshttps://doi.org/10.3762/bjoc.16.154openalex-snapshot
Three new O -isocrotonyl-3-hydroxybutyric acid congeners produced by a sea anemone-derived marine bacterium of the genus Vibrio
inferred← citeshttps://doi.org/10.3762/bjoc.16.97openalex-snapshot
A cyclopeptide and three oligomycin-class polyketides produced by an underexplored actinomycete of the genus Pseudosporangium
inferred← citeshttps://doi.org/10.3762/bjoc.17.203openalex-snapshot
Unsaturated fatty acids and a prenylated tryptophan derivative from a rare actinomycete of the genus Couchioplanes
inferred← citeshttps://doi.org/10.3762/bjoc.17.48openalex-snapshot
Menthyl esterification allows chiral resolution for the synthesis of artificial glutamate analogs
inferred← citeshttps://doi.org/10.3987/com-22-14640openalex-snapshot
Supramolecular Chirogenesis in Amide-Linked Bis(Zinc Porphyrin): Application for Absolute Configurational Assignment of Chiral Calboxylic Acids and Chiral Amino Acids
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