DOI: 10.1039/A701629H
(Paper)
Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1997, 1911-1912
Convergent, enantioselective synthesis of the novel furanoditerpene (+)-taonianone through facially selective chiral olefin–ketene [2+2] cycloaddition
(Note: The full text of this document is currently only available in the PDF Version )
Alice Kanazawa, Philippe Delair, Mehrnaz Pourashraf and Andrew E. Greene
Abstract
(+)-Taonianone, an unusual diterpene from the brown alga Taonia australasica, has been enantioselectively prepared through [2+2] cycloaddition of chloromethylketene with a chiral enol ether.
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