333788-75-3Relevant academic research and scientific papers
Enantioselective total synthesis of (+)-rogioloxepane A
Crimmins, Michael T.,DeBaillie, Amy C.
, p. 3009 - 3011 (2007/10/03)
(Matrix presented) The enantioselective synthesis of (+)-rogioloxepane A has been achieved in 21 steps from 1,5-hexadien-3-ol. The key steps in the synthesis are an asymmetric glycolate alkylation leading to the diene 2 and a subsequent ring-closing metat
The first total synthesis of (+)-rogioloxepane A
Matsumura, Ryuji,Suzuki, Toshio,Hagiwara, Hisahiro,Hoshi, Takashi,Ando, Masayoshi
, p. 1543 - 1546 (2007/10/03)
The first total synthesis of (+)-rogioloxepane A is described. The α,ω-trans-disubstituted oxepene skeleton was stereoselectively constructed via cyclization of the hydroxy epoxide promoted by the (Bu3Sn)2O/Zn(OTf)2 system. The proposed configurations of 6R and 13R were confirmed through this synthetic study.
