927834-93-3Relevant articles and documents
Ni(I)-Catalyzed Reductive Cyclization of 1,6-Dienes: Mechanism-Controlled trans Selectivity
Kuang, Yulong,Anthony, David,Katigbak, Joseph,Marrucci, Flaminia,Humagain, Sunita,Diao, Tianning
supporting information, p. 268 - 280 (2017/09/05)
A Ni-catalyzed reductive cyclization of 1,6-dienes affords 3,4-disubstituted cyclopentane and pyrrolidine derivatives with high trans diastereoselectivity. This cyclization reaction enables the efficient synthesis of trans-3,4-dimethyl gababutin, a pharma