Journal article

Total synthesis of ( )-crocacin C

TK Chakraborty, S Jayaprakash

Organic Letters | Published : 2000

Abstract

(matrix presented) The first asymmetric synthesis of (+)-crocacin C (3) is described which served to confirm the absolute configuration of this compound. The key step in the sequence was the stereoselective assembly of the (E, E)-diene amide side chain by a Stille cross-coupling between the stannane 5 and vinyl iodide 6.

University of Melbourne Researchers