A stereo controlled route to a key intermediate fro the synthesis of maytansine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Progress toward the total synthesis of maytansine. A stereoselective synthesis of the C-1 to C-7 moiety (northern zone)
2. Progress toward the total synthesis of maytansine. A model system containing the C-7 to C-16 moiety (southern and eastern zone)
3. Stereocontrolled route to a key intermediate for the synthesis of maytansine
4. Maytansinoids. Synthesis of a fragment of known absolute configuration involving chiral centers C-6 and C-7
5. Progress toward the total synthesis of maytansinoids. A facile route to the aromatic moiety (western zone)
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2. The chemistry and biology of the maytansinoid antitumor agents;Comptes Rendus Chimie;2008-11
3. Tris(ethylthio)borane;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. Ansamacrolides;Recent Progress in the Chemical Synthesis of Antibiotics;1990
5. Model studies for the total synthesis of the maytansinoids based on the intramolecular nitrile oxide-olefin [3+2] cycloaddition reaction;Tetrahedron;1985-01
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