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Title: Total synthesis of (+)-trans-195A. Author: Holub N, Neidhöfer J, Blechert S. Journal: Org Lett; 2005 Mar 31; 7(7):1227-9. PubMed ID: 15787473. Abstract: [reaction: see text] The first enantioselective synthesis of (+)-trans-195A is described. The structure has been constructed by ring-rearrangement metathesis (RRM) and zirconium-mediated Negishi-coupling, used for the first time to prepare 6,6-membered heterocycles, as key steps. By comparison of the synthesized material with the isolated natural product, the absolute configuration of natural trans-195A was determined to be (2R,4aS,5R,8aS)-(-).[Abstract] [Full Text] [Related] [New Search]