Baylis-Hillman reactions of 2-(trifluoroacetyl)-1,3-azoles.

[摘要]：under Baylis-Hillman reaction conditions to afford heterocyclic trifluoromethyl-contg. allylic alcs. in 36-97% yields. The thus obtained Baylis-Hillman adducts readily undergo Michael addn. reactions with various nucleophiles.

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