A carbonylative cross-coupling strategy to the total synthesis of the sarcodictyins: preliminary studies and synthesis of a cyclization precursor-Reference-Cited by-同舟云学术

A carbonylative cross-coupling strategy to the total synthesis of the sarcodictyins: preliminary studies and synthesis of a cyclization precursor

Published:2001-10 Issue:42 Volume:42 Page:7421-7425
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ceccarelli Simona M,Piarulli Umberto,Telser Joachim,Gennari Cesare

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. For a comprehensive review on the chemistry and biology of Taxol® (paclitaxel), see: Nicolaou, K. C.; Dai, W.-M.; Guy, R. K. Angew. Chem., Int. Ed. Engl. 1994, 33, 15.

2. Isolation from the Mediterranean Stolonifern CoralSarcodictyon roseum of Sarcodictyin C, D, E, and F, novel diterpenodic alcohols esterified by (E)- or (Z)-N(1)-methylurocanic acid. Failure of the carbon-skeleton type as a classification criterion

3. Eleutherobin, a New Cytotoxin that Mimics Paclitaxel (Taxol) by Stabilizing Microtubules

4. Ciomei, M.; Albanese, C.; Pastori, W.; Grandi, M.; Pietra, F.; D'Ambrosio, M.; Guerriero, A.; Battistini, C. Proc. Am. Assoc. Cancer Res. 1997, 38, Abstract 30.

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