Journal of the Chemical Society. Chemical communications p. 1252 - 1253 (1982)
Update date:2022-08-04
Topics:
Ley, Steven V.
Murray, P. John
A short synthesis of the sesquiterpene hirsutene (1) has been developed in which the key step involved intramolecular cyclization of a β-oxoester to an alkene using N-phenylselenophthalimide and tin tetrachloride.
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Doi:10.1055/s-1982-30061
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(2005)
