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Updated: Mar 31, 2026

Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
Published on: September 8, 2013
Complementary isonitrile-based multicomponent reactions for the synthesis of diversified cytotoxic hemiasterlin
Giordano Lesma1, Ivan Bassanini, Roberta Bortolozzi
1Università di Milano, Dipartimento di Chimica, via Golgi 19, Milano, 20133, Italy. alessandra.silvani@unimi.it.
Abstract:
A small family of structural analogues of the antimitotic tripeptides, hemiasterlins, have been designed and synthesized as potential inhibitors of tubulin polymerization. The effectiveness of a multicomponent approach was fully demonstrated by applying complementary versions of the isocyanide-based Ugi reaction. Compounds strictly related to the lead natural products, as well as more extensively modified analogues, have been synthesized in a concise and convergent manner. In some cases, biological evaluation provided evidence for strong cytotoxic activity (six human tumor cell lines) and for potent inhibition of tubulin polymerization.
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