Logo image
Sign in
Concise Pathway to New Multifunctionalized Constrained Pentacin Derivatives by Means of Two Stereospecific Tandem Reactions
Journal article   Peer reviewed

Concise Pathway to New Multifunctionalized Constrained Pentacin Derivatives by Means of Two Stereospecific Tandem Reactions

Thibault Coursindel, Jean Martinez and Isabelle Parrot
European Journal of Organic Chemistry, pp.4519-4522
2011

Abstract

Amino acids Heterocycles Diastereoselectivity Ring contraction Fused-ring systems
Starting from Boc-activated diketopiperazines, original bicyclic derivatives of trans- and cis-2-aminocyclopentanecarboxylic acid were prepared by using two stereospecific tandem reactions. One of them is a tandem transannular rearrangement of activated lactams/alkylation process leading to the stereoselective synthesis of suitably chiral pyrrolidine2,4-diones, allowing subsequent Michael-initiated ring closure, a simple and concise route to original multifunctionalized alicyclic β-amino esters.
url
Find in HALView

Metrics

1 Record Views

Details

Logo image