A new approach to the synthesis of functionalized pyrido[2,3-b]indoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C-9a positions-Reference-Cited by-同舟云学术

A new approach to the synthesis of functionalized pyrido[2,3-b]indoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C-9a positions

Published:1998-04 Issue:15 Volume:39 Page:2119-2122
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Abouabdellah Ahmed,Dodd Robert H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Grossularine-1 and grossularine-2, cytotoxic α-carbolines from the tunicate: Dendrodoa grossularia

2. Structure of mescengricin, a novel neuronal cell protecting substance produced by Streptomyces griseoflavus

3. Synthesis and potential anxiolytic activity of 4-amino-pyrido[2,3-b]indoles

4. An expeditious synthesis of structural analogs of the marine cytotoxic agents grossularines-1 and -2

5. Total synthesis of grossularines-1 and -2

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