Synthesis of Diversely Functionalized Hexahydropyrrolo[2,3-b]indoles Using Domino Reactions, Olefination, Isomerization and Claisen Rearrangement Followed by Reductive Cyclization-Reference-Cited by-同舟云学术

Synthesis of Diversely Functionalized Hexahydropyrrolo[2,3-b]indoles Using Domino Reactions, Olefination, Isomerization and Claisen Rearrangement Followed by Reductive Cyclization

Published:2005-03-09 Issue:8 Volume:70 Page:2957-2966
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kawasaki Tomomi¹,Ogawa Atsuyo¹,Terashima Romi¹,Saheki Toshiko¹,Ban Naoko¹,Sekiguchi Hiroko¹,Sakaguchi Ken-ei¹,Sakamoto Masanori¹

Affiliation:

1. Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo040289t

Reference61 articles.

1. Urochordamines A and B: Larval settlement/metamorphosis-promoting, pteridine-containing physostigmine alkaloids from the tunicate Ciona savignyi

2. Asperazine, a Selective Cytotoxic Alkaloid from a Sponge-Derived Culture of Aspergillus niger

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