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Journal ArticleDOI

Alkylation of amino acids without loss of the optical activity: preparation of .alpha.-substituted proline derivatives. A case of self-reproduction of chirality

Dieter Seebach, +3 more
- 22 Nov 1983 - 
- Vol. 105, Iss: 16, pp 5390-5398
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TLDR
In this article, an enolate par condensation de proline avec le pivalaldehyde suivie de deprotonation is described. André et al. describe the reactions of this enolate avec divers electrophiles.
Abstract
Preparation d'un enolate par condensation de proline avec le pivalaldehyde suivie de deprotonation. Etude des reactions de cet enolate avec divers electrophiles. Condensation du pivalaldehyde avec d'autres aminoacides

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Journal ArticleDOI

Proline-Catalyzed Direct Asymmetric Aldol Reactions

TL;DR: The finding that the amino acid proline is an effective asymmetric catalyst for the direct aldol reaction between unmodified acetone and a variety of aldehydes is reported.
Journal ArticleDOI

Structure and Reactivity of Lithium Enolates. From Pinacolone to Selective C‐Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures

TL;DR: The chemistry of lithium enolates is used to demonstrate that complex structures held together by noncovalent bonds (supramolecules) may dramatically influence the result of seemingly simple standard reactions of organic synthesis as mentioned in this paper.
Journal ArticleDOI

Total synthesis of (+)-11,11'-dideoxyverticillin A.

TL;DR: This work reports a concise enantioselective total synthesis of (+)-11,11′-dideoxyverticillin A via a strategy inspired by the biosynthetic hypothesis for this alkaloid through a rapid functionalization of the advanced molecular framework.
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