Enantioselective synthesis of α-amino esters through Petasis borono-Mannich multicomponent reaction of potassium trifluoroborate salts

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Abstract

Enantioselective synthesis of α-amino esters have been achieved through the Petasis borono-Mannich multicomponent reaction using (R)-BINOL-derived catalysts with stable heteroaryl and alkenyl trifluoroborate salts under mild conditions. The reaction provides direct access to optically active α-amino esters with moderate to good yields and enantioselectivities.

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Tong, M., Bai, X., Meng, X., Wang, J., Wang, T., Zhu, X., & Mao, B. (2019). Enantioselective synthesis of α-amino esters through Petasis borono-Mannich multicomponent reaction of potassium trifluoroborate salts. Journal of Chemical Research, 43(11–12), 557–564. https://doi.org/10.1177/1747519819876822

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