Preparation and 1,3-Dipolar Cycloaddition Reactions of β-Carboline Azomethine Ylides: A Direct Entry into C-1- and/or C-2-Functionalized Indolizino[8,7-b]indole Derivatives-Reference-Cited by-同舟云学术

Preparation and 1,3-Dipolar Cycloaddition Reactions of β-Carboline Azomethine Ylides: A Direct Entry into C-1- and/or C-2-Functionalized Indolizino[8,7-b]indole Derivatives

Published:1996-01-01 Issue:7 Volume:61 Page:2273-2282
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Poissonnet Guillaume¹,Théret-Bettiol Marie-Hélène¹,Dodd Robert H.¹

Affiliation:

1. Institut de Chimie des Substances Naturelles, Centre National de la Recherche Scientifique, 91198 Gif-sur-Yvette Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo951520t

Reference47 articles.

1. A QUEBRACHAMINE MODEL

2. Total synthesis of indole and dihydroindole alkaloids. V. Total synthesis of dl-quebrachamine and dl-aspidospermidine. General entry into the aspidosperma alkaloids

3. Total synthesis of indole and dihydroindole alkaloids. IV. Total synthesis of dl-dihydrocleavamine, dl-carbomethoxydihydrocleavamine, dl-coronaridine, dl-dihydrocatharanthine, and dl-ibogamine. General entry into the iboga and vinca alkaloids

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