About: (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives

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About: (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) wüsseschaftlicher Artikel, wo im März 2000 veröffentlicht worden isch (gsw) im März 2000 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в березні 2000 (uk) article scientifique publié en 2000 (fr) artículu científicu espublizáu en marzu de 2000 (ast) scientific article published on 01 March 2000 (en)
publication date	wds:Q73645709-9B626C37-42C9-4BD6-9563-89A87E381E74
publication date	2000-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73645709-0009CFAF-42ED-41DC-A6B1-9C28AEA7D0E6 wds:Q73645709-4FE1F317-A0AF-4AA6-863C-2D7B5B72C7FD wds:Q73645709-F217DBF3-6D08-4746-AA56-58D0ADA04D2F
author name string	V J Hruby C Cai V A Soloshonok
rdfs:label	(S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (en) (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (nl)
skos:prefLabel	(S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (en) (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (nl)
name	(S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (en) (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (nl)
title	wds:Q73645709-C47C09D8-E675-4F24-A158-C61DC2430228
title	(S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives (en)
page(s)	wds:Q73645709-07074F9B-99CA-4C51-B646-968220A32E9E
page(s)	747-750
instance of	wds:Q73645709-83D55D7D-C7B6-4E86-ACC7-80002003A26D
instance of	scholarly article
PubMed ID	wds:Q73645709-521BBA2A-1FF0-4204-B954-7976F9FE6AF4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10754676
PubMed ID	10754676
published in	wds:Q73645709-D1FEDE10-DDCF-4702-A7B6-83060841C2CA
published in	Organic Letters
issue	wds:Q73645709-E866E808-072F-4EBE-B22C-CE2475F69390
volume	wds:Q73645709-7F73F76E-C781-46C5-A60E-2DD2CF088063
issue	6
volume	2
DOI	wds:Q73645709-25AC4888-D4CF-4336-83D5-C3E79DBDBB1D
DOI	http://dx.doi.org/10.1021/OL990402F
DOI	10.1021/OL990402F
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73645709
is cites work of	Biological and conformational study of beta-substituted prolines in MT-II template: steric effects leading to human MC5 receptor selectivity Organic chemistry and biology: chemical biology through the eyes of collaboration Enhanced stereoselectivity of a Cu(II) complex chiral auxiliary in the synthesis of Fmoc-L-γ-carboxyglutamic acid Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographicall Modern Approaches for Asymmetric Construction of Carbon-Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs. Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)-O and Ni(II)-N coordination bonds Michael addition reactions of chiral glycine Schiff base Ni (II)-complex with 1-(1-phenylsulfonyl)benzene Axially chiral Ni(II) complexes of α-amino acids: Separation of enantiomers and kinetics of racemization. Asymmetric Synthesis of 4,4-(Difluoro)glutamic Acid via Chiral Ni(II)-Complexes of Dehydroalanine Schiff Bases. Effect of the Chiral Ligands Structure on the Stereochemical Outcome Preparative Method for Asymmetric Synthesis of (S)-2-Amino-4,4,4-trifluorobutanoic Acid Tandem Alkylation-Second-Order Asymmetric Transformation Protocol for the Preparation of Phenylalanine-Type Tailor-Made α-Amino Acids
is cites work of	wds:Q42044559-AC9EE3BD-D18A-4F60-8DBA-9158B25C6CEC wds:Q36436630-4B5AA0BE-8455-4E97-9EC6-80C5268EB5AC wds:Q89520719-16CC89F2-30FF-408B-B972-65D7FD3DF56A wds:Q92939161-5B34DC89-866C-4D0C-8909-74BEB42E19E7 wds:Q91964274-ABECCDD7-DD45-4F13-979D-873AF9F8FA9D wds:Q34583191-09CADE34-0FCF-4E74-8CFC-558FB5BB9A6F wds:Q36370739-0F28516A-37B6-4D72-97D2-C406DBE0B149 wds:Q89857923-711C4E38-F60B-496F-962C-20130566970E wds:Q40580707-142B36C7-B548-4E80-971F-B886285F60B2 wds:Q52613842-FAEED10B-8CC2-4B47-BBC6-1F1977C7AD73 wds:Q48044371-75581C15-54F6-491C-BF1F-D7C8E762DB02

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