253435-21-1Relevant articles and documents
Application of Hantzsch Ester and Meyer Nitrile in Radical Alkynylation Reactions
Liu, Xu,Liu, Ruoyu,Dai, Jie,Cheng, Xu,Li, Guigen
supporting information, p. 6906 - 6909 (2018/10/25)
The first example of constructing a Csp3-Csp bond with substituted Hantzsch ester and Meyer nitrile is reported. When benziodoxole-activated alkyne was applied as the alkynyl donor, products containing Csp3-Csp bonds involving primary, secondary, and tertiary carbon centers were achieved in up to 97% yields. K2S2O8 was the optimum radical initiator in this reaction.