Please use this identifier to cite or link to this item: 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

Files in This Item:
File Description SizeFormat 
research.0293.pdf2.21 MBAdobe PDFThumbnail
View/Open

SCOPUSTM   
Citations 50

10
Updated on Mar 24, 2025

Page view(s)

112
Updated on Mar 26, 2025

Download(s)

10
Updated on Mar 26, 2025

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.