100337-63-1Relevant articles and documents
Pd-Catalyzed Oxidative Heck Reaction of Grignard Reagents with Diaziridinone as Oxidant
Dai, Qipu,Zhao, Baoguo,Yang, Yihui,Shi, Yian
supporting information, p. 5157 - 5161 (2019/07/04)
A novel Pd-catalyzed oxidative Heck reaction with readily available Grignard reagents using di-t-butyldiaziridinone as an oxidant has been developed. Various substituted olefins were obtained in 46-91% yields with high regioselectivity under mild reaction conditions.
A NOVEL ORTHO-SUBSTITUENT EFFECT ON FORMATION OF VINYL CATIONS IN THE PHOTOLYSIS OF VINYL BROMIDES
Kitamura, Tsugio,Muta, Tomonobu,Kobayashi, Shinjiro,Taniguchi, Hiroshi
, p. 643 - 644 (2007/10/02)
Introduction of a substituent into ortho-position of β-aryl group in a vinyl bromide resulted in the preferential formation of a vinyl cation in the photolysis.It is considered that the steric repulsion of β-aryl groups makes a convenient conformation for an electron transfer from the aromatic ring to the halogen atom in the radical pair.