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

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.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra06155e
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Yang-Ling Wang, Wei‐Yu Huang, Junbiao Chang, Cai-Guang Li et al.
RSC Advances
Axial and Atropisomeric Chirality Synthesis
article

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

Yang-Ling Wang, Wei‐Yu Huang, Junbiao Chang, Cai-Guang Li, Guo-Li Chai, Kangbao Zhong, Gongming Zhu
article en

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.

RSC AdvancesVol. 15(40)
Henan Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province
Openalex Percentile: Top 81%
Axial and Atropisomeric Chirality Synthesis
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