Synthesis of Tertiary Benzylic Nitriles via Nickel-Catalyzed Markovnikov Hydrocyanation of α-Substituted Styrenes
Yidan Xing, Rongrong Yu and Xianjie Fang*
*School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, People’s Republic of China, Email: fangxjsjtu.edu.cn
Y. Xing, R. Yu, X. Fang, Org. Lett., 2020, 22, 1008-1012.
DOI: 10.1021/acs.orglett.9b04554
see article for more reactions
Abstract
A nickel-catalyzed Markovnikov hydrocyanation of α-substituted styrenes enables the synthesis of tertiary benzylic nitriles in good yields. This Lewis-acid-free transformation features an unprecedented functional groups tolerance.
see article for more examples
Key Words
ID: J54-Y2020