An efficient and enantioselective total synthesis of naturally occurring L-783277

  • Choi, Hwan Geun; 
  • Son, Jung Beom; 
  • Park, Dong-Sik; 
  • Ham, Young Jin; 
  • Hah, Jung-Mi; 
  • 외 1명
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초록

Naturally occurring L-783277 which belongs to 14-membered resorcylic acid lactones (RALs) turned out to be a potent kinase inhibitor against MEK (MAP kinase kinase). We successfully accomplished efficient and enantioselective total synthesis of L-783277 based on convergent assembly of one aromatic unit and two chiral building blocks with efficient orthogonal protection-deprotection strategy. Three key steps composed of olefin cross metathesis, addition of acetylene derivative to aldehyde, and Yamaguchi macrolactonization were subsequently employed to construct the framework of L-783277. The optical rotation value of L-783277 is for the first time presented in this Letter. (C) 2010 Elsevier Ltd. All rights reserved.

키워드

enantioselectivity; synthesis; unclassified drug; chirality; aldehyde; lactone derivative; article; deprotection reaction; alkene; l 783277; macrolactonization; acetylene; RESORCYLIC ACID LACTONES; KINASE INHIBITORS; CHIRAL SYNTHESIS; HYPOTHEMYCIN; LL-Z1640-2; MACROLIDES; PRODUCTS; POTENT; FUNGUS
제목
An efficient and enantioselective total synthesis of naturally occurring L-783277
저자
Choi, Hwan Geun; Son, Jung Beom; Park, Dong-Sik; Ham, Young Jin; Hah, Jung-Mi; Sim, Taebo
DOI
10.1016/j.tetlet.2010.07.122
발행일
2010-09
유형
Article
저널명
Tetrahedron Letters
권
51
호
38
페이지
4942 ~ 4946