An approach to the core skeleton of lancifodilactone F

Qiaoling Wang; Chuo Chen

doi:10.1021/ol800111j

An approach to the core skeleton of lancifodilactone F

Qiaoling Wang, Chuo Chen

Research output: Contribution to journal › Article › peer-review

54 Scopus citations

Abstract

Two cycloaddition reactions were utilized for the construction of the 5,6,7-tricyclic skeleton of lancifodilactone F and buxapentalactone. A [2+2] ketene cycloaddition reaction was first used to set their adjacent all-carbon quaternary centers at the 5,6-ring junction. An arene-olefin meta-photocycloaddition reaction was then used to install the 6- and 7-membered rings concurrently.

Original language	English (US)
Pages (from-to)	1223-1226
Number of pages	4
Journal	Organic Letters
Volume	10
Issue number	6
DOIs	https://doi.org/10.1021/ol800111j
State	Published - Mar 20 2008

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol800111j

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An approach to the core skeleton of lancifodilactone F

Abstract

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