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The enantioselectivity of the intramolecular asymmetric aldol reaction of 1,3-cycloheptanedione bearing a C-2 methyl substituent, mediated by a series of combinations of L-amino acid and Brønsted acid, was examined in detail.

chemical and pharmaceutical bulletin/chemical and pharmaceutical bulletin

Enantioselective Intramolecular Aldol Reaction Mediated by a Combination of L-Amino Acid and Bronsted Acid to Construct a Bicyclic Enedione Containing a 7-Membered Ring