Reversal of diastereofacial selectivity in the nucleophilic addition reaction to chiral N-sulfinimine and application to the synthesis of indrizidine 223AB-Reference-Cited by-同舟云学术

Reversal of diastereofacial selectivity in the nucleophilic addition reaction to chiral N-sulfinimine and application to the synthesis of indrizidine 223AB

Published:2002-11 Issue:47 Volume:58 Page:9621-9628
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Koriyama Yuji,Nozawa Akihiro,Hayakawa Ryuuichirou,Shimizu Makoto

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate

2. Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group

3. Asymmetric synthesis of sulfinimines: Chiral ammonia imine synthons

4. Asymmetric induction in the reduction of optically active N-alkylidenesulphinamides by metal hydrides. A new, efficient enantioselective route to chiral amines

5. Stereoselective addition reactions of chiral N-benzylidene-p-toluenesulfinamides. Asymmetric syntheses of .beta.- and .gamma.-amino acids

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