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Total synthesis of (+/-)-crinine via the regioselective stille coupling and Diels-Alder reaction of 3,5-dibromo-2-pyrone
- Authors
- Tam, Nguyen Thanh; Cho, Cheon-Gyu
- Issue Date
- Feb-2008
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.10, no.4, pp.601 - 603
- Indexed
- SCIE
SCOPUS
- Journal Title
- ORGANIC LETTERS
- Volume
- 10
- Number
- 4
- Start Page
- 601
- End Page
- 603
- ISSN
- 1523-7060
- Abstract
- 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.
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Related Researcher
- Cho, Cheon Gyu
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)