Tocopherol side chain synthesis via asymmetric organocatalytic transfer hydrogenation and convenient measurement of stereoselectivity

  • Lee, Hyunji; 
  • Lee, You-Kyoung; 
  • Kim, Dong-Guk; 
  • Son, Mi-Sun; 
  • Nam, Tae-Gyu; 
  • 외 1명
Citations

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7
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7

초록

An asymmetric synthetic route for 1-iodofarnesane, a key intermediate for tocopherol side chain synthesis, starting from (+)-(R)-citronellal was developed. 1-Iodofamesane was prepared through eight steps in about 50% overall yield, and asymmetric transfer hydrogenation of the enal with a chiral organocatalyst was conducted as a stereoinduction step. To measure the stereoinduction level and optical purity of the product, a convenient analytical method was developed in which a phenylcarbamate derivative of the C-15 alcohol was found to be suitable to give proper polarity and UV-activity for chiral UV-HPLC analysis. (C) 2014 Elsevier Ltd. All rights reserved.

키워드

Tocopherol; Asymmetric synthesis; Organocatalyst; Stereoselectivity; UV-HPLC; BREAKING PHENOLIC ANTIOXIDANTS; VITAMIN-E; ALPHA-TOCOPHEROL; AMINOPYRIDINOL ANTIOXIDANTS; ENANTIOSELECTIVE SYNTHESIS; BIOLOGICAL MOLECULES; LIPID-PEROXIDATION; HANTZSCH ESTERS; DERIVATIVES; RADICALS
제목
Tocopherol side chain synthesis via asymmetric organocatalytic transfer hydrogenation and convenient measurement of stereoselectivity
저자
Lee, Hyunji; Lee, You-Kyoung; Kim, Dong-Guk; Son, Mi-Sun; Nam, Tae-Gyu; Jeong, Byeong-Seon
DOI
10.1016/j.tetlet.2014.08.085
발행일
2014-10
유형
Article
저널명
Tetrahedron Letters
권
55
호
43
페이지
5895 ~ 5897