Total synthesis of viridiofungin A
…, K Takahashi, J Ishihara, S Hatakeyama
Index: Morokuma, Kenji; Takahashi, Keisuke; Ishihara, Jun; Hatakeyama, Susumi Chemical Communications, 2005 , # 17 p. 2265 - 2267
Full Text: HTML
Citation Number: 11
Abstract
Viridiofungin A, a member of amino alkyl citrate antibiotics from Trichoderma viride, was enantioselectively synthesized in naturally occurring form for the first time, employing regio- and stereoselective opening of the chiral glycidate with vinylmagnesium bromide and alkene cross metathesis of the citric acid core and hexadec-15-en-8-one as key steps.
Related Articles:
[Garanti,L. et al. Gazzetta Chimica Italiana, 1976 , vol. 106, p. 187 - 196]
[Jacquier, R.; Lazaro, R.; Raniriseheno, H.; Viallefont, P. Tetrahedron Letters, 1984 , vol. 25, # 48 p. 5525 - 5528]
[Garanti,L. et al. Gazzetta Chimica Italiana, 1976 , vol. 106, p. 187 - 196]