Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates

The conversion of vinyl-substituted 6- and 7-membered cyclic carbonates into 8- and 9-membered medium-ring lactones has been achieved in good yield using dimethyltitanocene in toluene at reflux. The reaction proceeds by initial formation of a ketene acetal which undergoes subsequent in situ Claisen...

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Bibliographic Details
Main Authors: Anderson, E, Davidson, J, Harrison, JR, O'Sullivan, P, Burton, J, Collins, I, Holmes, AB
Format: Journal article
Language:English
Published: 2002