About: Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids

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About: Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1999 (uk) article scientifique publié en 1999 (fr) im September 1999 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57974680-99CEEDAD-2C6C-40C9-B7FF-0AF41291830E
publication date	1999-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57974680-FE9FDDC2-E5B2-4386-B9A2-DE10EE3CF2A2
language of work or name	English
cites work	wds:Q57974680-3D3AD38A-9896-4899-9BA9-68060952C150 wds:Q57974680-4BA0B6AD-6C4C-4C83-8343-8DE41A570D79 wds:Q57974680-4E9DFDBF-45C6-4361-A80F-FD3D17C8D78C
cites work	Highly enantioselective synthesis of cyclic and functionalized α-amino acids by means of a chiral phase transfer catalyst The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions
author name string	wds:Q57974680-3AF66918-AE1A-457C-91C6-CA5AEBD23BE0 wds:Q57974680-94B4110D-908C-4FC4-8A76-3ED6FF347749 wds:Q57974680-D00C0012-1FC8-4D6B-A3C3-BEA1C5476C8C wds:Q57974680-E866AB05-2D23-4429-B613-570CCBFC742B wds:Q57974680-EE8F9C91-4F86-4C17-81A3-82B448465478
author name string	Concepción Pedregal Isabel Merino Josefa Flórez Jesús Ezquerra María-Amparo Llorca
rdfs:label	Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (en) Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (nl)
skos:prefLabel	Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (en) Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (nl)
name	Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (en) Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids (nl)
author	wds:Q57974680-AF44FB1D-F19C-4507-9E4B-A3778DB7F542 wds:Q57974680-CF322B1A-FDEE-48DB-B215-C185A4496A66
author	José Barluenga Santiago García-Granda
title	wds:Q57974680-4CF1463F-93B9-4929-9CD1-AC7B9A48E7BE
title	Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of beta-Substituted Glutamic Acids (en)
page(s)	wds:Q57974680-176D38A9-E0A2-4273-92B4-9377930855DC
page(s)	6554-6565
instance of	wds:Q57974680-0A789AB5-8C76-4268-AFAB-DDAE1EFEE6C0
instance of	scholarly article
main subject	wds:Q57974680-A84E5E89-4844-4683-B5AA-D3BF933E3B31 wds:Q57974680-C6C139B3-AAE5-4440-A04D-A522A7A8AD3D
main subject	stereoselectivity chirality
PubMed ID	wds:Q57974680-9A2D0E9A-AC13-4BC4-8E47-202A62137A7E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11674657
PubMed ID	11674657
published in	wds:Q57974680-C485B294-5711-497B-88E2-F74B4030DC53
published in	Journal of Organic Chemistry
issue	wds:Q57974680-3BAA78C1-EBDB-4B52-AB75-33A048C41D90
volume	wds:Q57974680-AEF2AF1C-E4D9-4A93-B29F-4D3D3BA0BC82
issue	18
volume	64
DOI	wds:Q57974680-E6E25DF3-3901-4CAC-83D7-70758D1DA55C
DOI	http://dx.doi.org/10.1021/JO9819739
DOI	10.1021/JO9819739
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57974680
is cites work of	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 Asymmetric synthesis of anti- and syn-2,3-diamino esters using sulfinimines. Water and concentration effects Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines. Direct catalytic asymmetric synthesis of N-heterocycles from commodity acid chlorides by employing α,β-unsaturated acylammonium salts Diastereoselective synthesis of cycloheptadienol derivatives by a formal [5+2] carbocyclization reaction of alpha,beta,gamma,delta-diunsaturated (methoxy)carbene complexes with methyl ketone lithium enolates
is cites work of	wds:Q42044559-27B889C6-F69A-4270-86A9-C71B16D478DD wds:Q49034242-84DCBF4B-1E5A-45B9-B6FA-5F2EFEEC094E wds:Q46568743-D3A898DB-F277-4C97-97A8-86DCD074BF09 wds:Q34607289-6ADB89E1-5FE7-44FD-85F0-062B6D7B3235 wds:Q45106659-5E379394-C948-44E5-ADC6-47C3E3B1057A

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