906624-08-6Relevant academic research and scientific papers
Total synthesis of methyl sarcophytoate, a marine natural biscembranoid
Ichige, Takahiro,Okano, Yusuke,Kanoh, Naoki,Nakata, Masaya
supporting information; experimental part, p. 230 - 243 (2009/04/18)
(Chemical Equation Presented) The total synthesis of methyl sarcophytoate (1), a marine natural biscembranoid, has been achieved by the thermal Diels-Alder reaction between the 14-membered dienophile unit, methyl sarcoate (2), and the 14-membered diene unit 64. Methyl sarcoate (2) was prepared using n-BuLi-Bu2Mg-mediated dithiane coupling, Kosugi-Migita-Stille coupling, and Grubbs ring-closing metathesis. The diene unit 64 was prepared using Sharpless asymmetric epoxidation, Grubbs ring-closing metathesis, 6-exo-tet epoxide opening, and n-BuLi-Bu2Mg-mediated Ito-Kodama cyclization. The final Diels-Alder reaction between 2 and 64 proceeded with high site, endo/exo, π-face, and regioselectivities. During this reaction, partial E → Z isomerization at the C4 position was observed.
Total synthesis of methyl sarcophytoate
Ichige, Takahiro,Okano, Yusuke,Kanoh, Naoki,Nakata, Masaya
, p. 9862 - 9863 (2008/02/13)
Together with the improved synthesis of the diene unit 15 of methyl sarcophytoate (1), a biscembranoid marine natural product, the asymmetric total synthesis of 1 was achieved by the thermal Diels-Alder reaction between the dienophile unit, methyl sarcoat
