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May 21, 2026
Enantioselective Addition of Thiols to Pyrazolone Ketimines by Cinchona Alkaloid-Derived C-2′ Amino Organocatalyst
YW
Yakun Wang
XD
Xiaoyu Du
Nanjing University of Science and Technology
XK
Xu Kong
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Key Points
The aim is to explore the enantioselective addition of thiols to pyrazolone ketimines using a specific organocatalyst.
Utilized cinchona alkaloid-derived C-2′ amino organocatalysts for asymmetric synthesis.
Examined reaction conditions to optimize yields and enantioselectivity.
Analyzed the outcomes based on chiral materials.
Achieved high enantioselectivity with specific yield percentages.
Performed quantitative analysis demonstrating effective chiral construction.
Indicated significant potential for developing new synthetic methodologies.
Abstract
The asymmetric construction of chiral
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Enantioselective Addition of Thiols to Pyrazolone Ketimines by Cinchona Alkaloid-Derived C-2′ Amino Organocatalyst | Synapse
Cite This Study
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Wang et al. (Mon,) studied this question.
synapsesocial.com/papers/6a0ea02cbe05d6e3efb5f0b2
https://doi.org/https://doi.org/10.1021/acs.orglett.6c01431