Lithiation of aliphatic 1-acylbenzotriazoles with subsequent reaction with alpha,beta-unsaturated ketones and aldehydes affords either 3,4,6-trisubstituted 3,4-dihydropyran-2-ones or 1,3-dienes depending on the carbonyl reagent used. Substituent effects on product yield and isomer ratio are discussed.
No takes yet. Share an insight, caveat, or question.
Katritzky et al. (2002) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: