Hydrogen atom transfer methodology for the synthesis of C-22, C-23, and C-25 stereoisomers of cephalostatin north 1 side chain from spirostan sapogenins-Reference-Cited by-同舟云学术

Hydrogen atom transfer methodology for the synthesis of C-22, C-23, and C-25 stereoisomers of cephalostatin north 1 side chain from spirostan sapogenins

Published:2005-03 Issue:11 Volume:61 Page:2803-2814
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Betancor Carmen,Freire Raimundo,Pérez-Martín Inés,Prangé Thierry,Suárez Ernesto

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference76 articles.

1. Antineoplastic agents. 147. Isolation and structure of the powerful cell growth inhibitor cephalostatin 1

2. Antineoplastic Agents. 398. Isolation and Structure Elucidation of Cephalostatins 18 and 19

3. Ritterazine A, a highly cytotoxic dimeric steroidal alkaloid, from the tunicate Ritterella tokioka

4. Isolation and structure elucidation of ritterazines B and C, highly cytotoxic dimeric steroidal alkaloids, from the tunicate Ritterella tokioka

5. Ten more ritterazines, cytotoxic steroidal alkaloids from the tunicate Ritterella tokioka

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