Total synthesis of (+/-)-crinine via the regioselective stille coupling and Diels-Alder reaction of 3,5-dibromo-2-pyrone

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초록

The regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-methylenedioxyphenyl)-5-bromo-2-pyrone provided a new synthetic route to crinine. The vinyl bromide group can be used as a handle for further derivatization.

키워드

AMARYLLIDACEAE ALKALOIDSCYCLOADDITIONS
제목
Total synthesis of (+/-)-crinine via the regioselective stille coupling and Diels-Alder reaction of 3,5-dibromo-2-pyrone
저자
Tam, Nguyen ThanhCho, Cheon-Gyu
DOI
10.1021/ol702907u
발행일
2008-02
유형
Article
저널명
Organic Letters
10
4
페이지
601 ~ 603