Unprecedented Stereospecific Synthesis of a Novel Tetracyclic Ring System, a Hybrid of Tetrahydropyrrolo[2,3-b]indole and Tetrahydroimidazo[1,2-a]indole, via a Domino Reaction upon a Tryptophan-Derived Amino Nitrile-Reference-Cited by-同舟云学术

Unprecedented Stereospecific Synthesis of a Novel Tetracyclic Ring System, a Hybrid of Tetrahydropyrrolo[2,3-b]indole and Tetrahydroimidazo[1,2-a]indole, via a Domino Reaction upon a Tryptophan-Derived Amino Nitrile

Published:2004-07-14 Issue:16 Volume:6 Page:2641-2644
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

González-Vera Juan A.¹,García-López M. Teresa¹,Herranz Rosario¹

Affiliation:

1. Instituto de Química Médica (CSIC), Juan de la Cierva 3, E-28006 Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol049222i

Reference45 articles.

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2. Marine alkaloids. 2. Bromo alkaloids from a marine bryozoan Flustra foliacea. Isolation and structure elucidation

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

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