Diastereoselective synthesis of substituted 2,3,4,5-tetrahydro-1H-1-benzazepine-5-carboxylic esters by a tandem reduction-reductive animation reaction-Reference-Cited by-同舟云学术

Diastereoselective synthesis of substituted 2,3,4,5-tetrahydro-1H-1-benzazepine-5-carboxylic esters by a tandem reduction-reductive animation reaction

Published:2004-07 Issue:4 Volume:41 Page:563-568
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Bunce Richard A.,Johnson Lara B.,Holt Elizabeth M.

Publisher

Wiley

Subject

Organic Chemistry

Reference34 articles.

1. Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction−Reductive Amination Reaction

2. Azepine Ring Systems Containing two Rings

3. Syntheses and conformational analyses of some 3-amino-2,5-dioxo-2,3,4,5-tetrahydro-1H-1-benzazepine derivatives: X-ray crystal structure of 35-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2,5-dioxo-2,3,4,5-tetrahydro-1H-1-benzazepine

4. Synthesis of optically active α-aminobenzolactam via an oxidative–cyclization reaction

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