Lewis acid-mediated SN2 type displacement by grignard reagents on chiral perhydropyrido[2,1-b]pyrrolo[1,2-d][1,3,4]oxadiazine. Chirality induction in asymmetric synthesis of 2-substituted piperidines-Reference-Cited by-同舟云学术

Lewis acid-mediated SN2 type displacement by grignard reagents on chiral perhydropyrido[2,1-b]pyrrolo[1,2-d][1,3,4]oxadiazine. Chirality induction in asymmetric synthesis of 2-substituted piperidines

Published:1997-06 Issue:26 Volume:38 Page:4623-4626
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yamazaki Naoki,Kibayashi Chihiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Organometallic reactions characteristic of chiral heterocyclic compounds: Synthesis and stereoselective grignard reaction of chiral 4-Oxa-7,7a-diazaperhydroindans.

2. A simple asymmetric synthesis of 2-substituted pyrrolidines and 5-substituted pyrrolidinones

3. Chiral precursors for the synthesis of enantiomerically pure piperidines. Total synthesis of (R)-(-)-coniine

4. An Asymmetric Route to Chiral, Nonracemic 2-Substituted Piperidines. Synthesis of (-)-Pipecoline, (+)-Coniine, and (-)-Coniceine

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