Total synthesis of cryptophycin-24 (arenastatin A) amenable to structural modifications in the C16 side chain

M. Eggen, C. J. Mossman, S. B. Buck, S. K. Nair, L. Bhat, S. M. Ali, E. A. Reiff, T. C. Boge, G. I. Georg

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

Two efficient protocols for the synthesis of tert-butyl (5S,6R,2E,7E)-5-[(tert-butyldimethylsilyl)-oxy]-6-methyl-8-phenyl-2,7-octadie noate, a major component of the cryptophycins, are reported. The first utilized the Noyori reduction and Frater alkylation of methyl 5-benzyloxy-3-oxopentanoate to set two stereogenic centers, which became the C16 hydroxyl and C1' methyl of the cryptophycins. The second approach started from 3-p-methoxybenzyloxypropanal and a crotyl borane reagent derived from (-)-α-pinene to set both stereocenters in a single step and provided the dephenyl analogue, tert-butyl (5S,6R,2E)-5-[(tert-butyldimethylsilyl)oxy]-6-methyl-2,7-octadienoate, in five steps. This compound was readily converted to the 8-phenyl compound via Heck coupling. The silanyloxy esters were efficiently deprotected and coupled to the C2-C10 amino acid fragment to provide desepoxyarenastatin A and its dephenyl analogue. The terminal olefin of the latter was further elaborated via Heck coupling. Epoxidation provided cryptophycin-24 (arenastatin A).

Original languageEnglish (US)
Pages (from-to)7792-7799
Number of pages8
JournalJournal of Organic Chemistry
Volume65
Issue number23
DOIs
StatePublished - Nov 17 2000

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