Functionalized chloroenamines in aminocyclopropane synthesis IV A synthesis for bicyclic lactams from carbamoylated chloroenamines - the result of a tandem ring contraction - cyclization process-Reference-Cited by-同舟云学术

Functionalized chloroenamines in aminocyclopropane synthesis IV A synthesis for bicyclic lactams from carbamoylated chloroenamines - the result of a tandem ring contraction - cyclization process

Published:1989-01 Issue:21 Volume:45 Page:6683-6696
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Vilsmaier Elmar,Adam Rainer,Altmeier Peter,Fath Joachim,Scherer Hans-Josef,Maas Gerhard,Wagner Oliver

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Functionalized chloroenamines in aminocyclopropane synthesis I. — bicyclic and pentacyclic lactams from carbamoylated chloroenamines

2. Use of cyclopropanes and their derivatives in organic synthesis

3. Vilsmaier, E.; Adam, R.; Tetzlaff, C.; Cronauer, R. Tetrahedron, in press.

4. 138. Fused carbon rings. Part X. Some fundamental properties of the 0 : 3 : 3-bicyclooctane ring

5. Enamines a halogene allylique—II

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