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https://hdl.handle.net/10356/179793
Title: | Access to axially chiral aryl aldehydes via carbene-catalyzed nitrile formation and desymmetrization reaction | Authors: | Cai, Yuanlin Lv, Ya Shu, Liangzhen Jin, Zhichao Chi, Robin Yonggui Li, Tingting |
Keywords: | Chemistry Engineering |
Issue Date: | 2024 | Source: | Cai, Y., Lv, Y., Shu, L., Jin, Z., Chi, R. Y. & Li, T. (2024). Access to axially chiral aryl aldehydes via carbene-catalyzed nitrile formation and desymmetrization reaction. Research, 7, 0293-. https://dx.doi.org/10.34133/research.0293 | Project: | NRF-NRFI2016-06 NRF-CRP22-2019-0002 RG7/20 RG70/21 MOE2019-T2-2-117 MOE2018-T3-1-003 |
Journal: | Research | Abstract: | An approach utilizing N-heterocyclic carbene for nitrile formation and desymmetrization reaction is developed. The process involves kinetic resolution, with the axially chiral aryl monoaldehydes obtained in moderate yields with excellent optical purities. These axially chiral aryl monoaldehydes can be conveniently transformed into functionalized molecules, showing great potential as catalysts in organic chemistry. | URI: | https://hdl.handle.net/10356/179793 | ISSN: | 2096-5168 | DOI: | 10.34133/research.0293 | Schools: | School of Chemistry, Chemical Engineering and Biotechnology | Rights: | © 2024 Yuanlin Cai et al. Exclusive licensee Science and Technology Review Publishing House. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0). | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | CCEB Journal Articles |
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research.0293.pdf | 2.21 MB | Adobe PDF | ![]() View/Open |
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