Journal
ORGANIC LETTERS
Volume 7, Issue 14, Pages 2849-2852Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0505959
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A formal enantioselective synthesis of allocolchicine and a synthesis of a C-ring analogue have been achieved by employing an intramolecular direct arylation of an aryl chloride to form the biaryl carbon-carbon bond and the seven-membered ring.
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