Zinc chloride induced stereoselection in syntheses of α-amino-β-hydroxy acid derivatives-Reference-Cited by-同舟云学术

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Zinc chloride induced stereoselection in syntheses of α-amino-β-hydroxy acid derivatives

Published:1991 Issue:10 Volume: Page:682-683
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

van der Werf Anne W.,Kellogg Richard M.,van Bolhuis F.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000682

Reference15 articles.

1. Über α‐Aminosäuren, I: Eine einfache Synthese für β‐Hydroxy‐α‐aminosäuren

2. A NEW METHOD FOR ENANTIOSELECTIVE SYNTHESIS OF β-HYDROXY-α-AMINO ACIDS

3. A facile cleavage of oxirane with hydrazoic acid in dmf A new route to chiral β-hydroxy-α-amino acids

4. Asymmetric synthesis of anti-β-hydroxy-α-amino acids

5. Stereoselective alkylation of chiral glycine enolate synthons. The enantioselective synthesis of α-amino acid derivatives.

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1. Zinc Chloride;Encyclopedia of Reagents for Organic Synthesis;2016-12-01

2. EthylN-(Diphenylmethylene)glycinate;Encyclopedia of Reagents for Organic Synthesis;2016-03-31

3. ChemInform Abstract: Zinc Chloride-Induced Stereoselection in Syntheses of α-Amino-. beta.-hydroxy Acid Derivatives.;ChemInform;2010-08-22

4. Zinc Chloride;Encyclopedia of Reagents for Organic Synthesis;2006-09-15

5. Zinc Chloride;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

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