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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
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7초록
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
- 발행일
- 2014-10
- 유형
- Article
- 권
- 55
- 호
- 43
- 페이지
- 5895 ~ 5897
- 언어
- ENG
- 출판사
- PERGAMON-ELSEVIER SCIENCE LTD
- 발행국가
- 영국
- 분량
- 3 페이지
- ISSN
- P 0040-4039