Asymmetric syntheses via heterocyclic intermediates, XL. Studies on the acylation of lithiated bislactim ethers of cyclo(-L-Val-Ala-) and cyclo(-L-Val-Gly-) Asymmetric synthesis of (R)-α-alkenyl and (R)-α-ethinyl alanine methyl esters by the bislactim ether method-Reference-Cited by-同舟云学术

Asymmetric syntheses via heterocyclic intermediates, XL. Studies on the acylation of lithiated bislactim ethers of cyclo(-L-Val-Ala-) and cyclo(-L-Val-Gly-) Asymmetric synthesis of (R)-α-alkenyl and (R)-α-ethinyl alanine methyl esters by the bislactim ether method

Published:1988-08-16 Issue:8 Volume:1988 Page:781-786
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Schöllkopf Ulrich,Westphalen Karl-Otto,Schröder Jürgen,Horn Klaus

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference19 articles.

1. Part 39: , , Tetrahedrron, in print.

2. Asymmetric syntheses of amino acids via metalated bis-lactim ethers of 2,5-diketopiperazines

3. – in Organic Synthesis: An Interdisciplinary Challenge (, , Eds.), p. 101, Blackwell Scientific Publication, Oxford, London, Edinburgh, Boston, Palo Alto, Melbourne 1985.

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