An ester enolate–Claisen rearrangement route to substituted 4-alkylideneprolines. Studies toward a definitive structural revision of lucentamycin A

S Ranatunga, JS Kim, U Pal…

Index: Ranatunga, Sujeewa; Kim, Jinsoo S.; Pal, Ujjwal; Del Valle, Juan R. Journal of Organic Chemistry, 2011 , vol. 76, # 21 p. 8962 - 8976

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Citation Number: 8

Abstract

Substituted 4-alkylideneprolines represent a rare class of naturally occurring amino acids with promising biological activities. Lucentamycin A is a cytotoxic, marine-derived tripeptide that harbors a 4-ethylidine-3-methylproline (Emp) residue unique among known peptide natural products. In this paper, we examine the synthesis of Emp and related 4- alkylideneprolines employing a versatile ester enolate–Claisen rearrangement. The ...