Catalytic and Enantioselective Diels-Alder Reactions of (E)-4-Oxopent-2-enoates.

Org Lett

Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science, College of Chemistry and Molecular Engineering, and Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.

Published: August 2017

Novel oxazaborolidines activated by the strong acid triflimide or AlBr form cationic chiral catalysts. These are effective catalysts for highly regio- and enantioselective Diels-Alder reactions using substituted (E)-4-oxopent-2-enoates as dienophiles.

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http://dx.doi.org/10.1021/acs.orglett.7b01692DOI Listing

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