56030-48-9Relevant articles and documents
Convenient synthesis of pyrrolidines by amphiphilic allylation of imines with 2-methylenepropane-1,3-diols
Kimura, Masanari,Tamaki, Takato,Nakata, Masanori,Tohyama, Katsumi,Tamaru, Yoshinao
supporting information; experimental part, p. 5803 - 5805 (2009/03/11)
(Chemical Equation Presented). A straightforward route: The combination of a palladium catalyst and triethylborane promotes the amphiphilic (nucleophilic-electrophilic) allylation of aldimines, prepared in situ from a wide variety of aromatic and aliphatic aldehydes and amines, with commercially available 2-methylenepropane-1,3-diols to provide pyrrolidines (see scheme).
An improved procedure for the preparation of the O,2-dianion of allyl alcohol
Hegde, Sayee G.,Myles, David C.
, p. 2111 - 2115 (2007/10/03)
An improved procedure for the preparation of the O,2-dianion of allyl alcohol is described. The use of the magnesium alkoxide of 2-bromopropen-1- ol instead of the known lithium salt, suppresses dehydrohalogenation upon treatment with tert-butyl lithium a