Oxidation, With Chiral Retention, of Benzyloxycarbonyl Threonine Methyl Ester-Reference-Cited by-同舟云学术

Oxidation, With Chiral Retention, of Benzyloxycarbonyl Threonine Methyl Ester

Published:1992-11 Issue:21 Volume:22 Page:3075-3079
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Delacotte Jean-Michel¹,Galons Hervé¹,Schott Dominique²,Morgat Jean-Louis²

Affiliation:

1. a U. F. R. des Sciences Pharmaceutiques et Biologiques , 4, Avenue de l'Observatoire, 75270 , Paris , France

2. b Service de Biochimie des Protéines, Laboratoire d'Ingénierie des Protéines , C. E. N. Saclay, 91190 , Gif sur Yvette , France

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397919209409256

Reference9 articles.

1. Synthesis of tritiated threonine with a high specific activity

2. Afonso , A. Chackalamannil , S. Fett , N. Ganguly , A. K. and Kirkup , M. 1989. “Recent Advances in the Chemistry of β-Lactam Antibiotics”, Edited by: Bentley , P. H. and Southgate , R. 295London: The Royal Society of Chemistry.

3. Dibenzylaminoacetates as useful synthetic equivalents of glycine in the synthesis of α-amino-β-hydroxyacids1

4. Stereoselective synthesis of cis-4-(substituted) monobactams from ethyl acetoacetate

5. Notiz zur Oxydation von N ‐Acyl‐serin‐ und ‐threonin‐Derivaten mit Blei(IV)‐acetat

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4. A new efficient synthesis of ethyl β-carboline-3-carboxylate (β-CCE) and methyl 4-methyl-β-carboline-3-carboxylate (4-methyl-β-CCM) starting fr;Tetrahedron;1994-01

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