A New Method for Cyclopentanone Annelation

DOI: 10.1021/jo00175a032

Source and publish data:

Journal of Organic Chemistry p. 153 - 157 (1984)

Update date:2022-08-05

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Authors:

Snider, Barry B.

Cartaya-Marin, Claudia P.

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Article abstract of DOI:10.1021/jo00175a032

MeAlCl2-initiated cyclization of enone 6d provides an 85percent yield of a 9:1 mixture of trans- and cis-fused hydroazulenones 9 and 10.Similarly, cyclization of 7d gives a 31percent yield of 11 with an equatorial methyl group, and cyclization of 8d affor

Full text of DOI:10.1021/jo00175a032

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