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Title: Studies directed toward the total synthesis of discodermolide: asymmetric synthesis of the C1-C14 fragment. Author: Arefolov A, Panek JS. Journal: Org Lett; 2002 Jul 11; 4(14):2397-400. PubMed ID: 12098256. Abstract: [structure: see text] A convergent and stereoselective assembly of the C1-C14 subunit of marine natural product (+)-discodermolide has been completed. The approach employs chiral allylsilane bond construction methodology to establish four of the eight stereogenic centers. Key fragment coupling is achieved via an efficient stereoselective acetate aldol reaction between C1-C6 and C7-C14 subunits.[Abstract] [Full Text] [Related] [New Search]