Issue 40, 2025, Issue in Progress

Chiral binaphthol-catalyzed enantioselective conjugate addition of alkenyl trifluoroborate salts to alkenyl-substituted benzothiazoles

Abstract

The chiral binaphthol-catalyzed enantioselective conjugate addition of alkenyl trifluoroborate salts to alkenyl-substituted benzothiazoles is reported, providing the 1,4-addition products in moderate to high yields and excellent enantioselectivities (up to >99% ee). This scalable catalytic system exhibits high efficiency and broad substrate scopes. Additionally, alkenyl-substituted benzoxazole was also compatible with standard conditions.

Graphical abstract: Chiral binaphthol-catalyzed enantioselective conjugate addition of alkenyl trifluoroborate salts to alkenyl-substituted benzothiazoles

Supplementary files

Article information

Article type
Paper
Submitted
20 Aug 2025
Accepted
08 Sep 2025
First published
15 Sep 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 33586-33591

Chiral binaphthol-catalyzed enantioselective conjugate addition of alkenyl trifluoroborate salts to alkenyl-substituted benzothiazoles

W. Huang, Y. Wang, C. Li, K. Zhong, G. Zhu, J. Chang and G. Chai, RSC Adv., 2025, 15, 33586 DOI: 10.1039/D5RA06155E

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