The development of a new bisguanidinium salt as a multifunctional organocatalyst for asymmetric cascade esterification/aza-Michael reaction between 2-hydroxyphenyl-substituted enones and isocyanates is reported. A high level of enantioinduction and excellent isolated yields were achieved under mild reaction conditions. Enantiomerically enriched 1,3-benzoxazin-2-ones were constructed, and a possible catalytic model was suggested based on the mechanism-driven experiments.

The new bisguanidinium salt effectively catalyzes the asymmetric cascade esterification/aza-Michael reaction between 2-hydroxyphenyl-substituted enones and isocyanates, resulting in enantiomerically enriched 1,3-benzo

Paper

Organocatalytic Asymmetric Cascade Reaction of 2-Hydroxyphenyl-Substituted Enones and Isocyanates To Construct 1,3-Benzoxazin-2-ones.

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