77629-05-1Relevant articles and documents
Copper-catalyzed regioselective fluorination of allylic halides
Zhang, Zuxiao,Wang, Fei,Mu, Xin,Chen, Pinhong,Liu, Guosheng
, p. 7549 - 7553 (2013)
Group activity: A novel copper-catalyzed fluorination of internal allylic bromides and chlorides has been developed by using Et3N×3 HF as the fluorine source. A functional group (FG) within the substrate is required to achieve the allylic fluorination, and a variety of secondary allylic fluoride compounds can be accessed in good yield with excellent regioselectivity. Copyright
New Methodology for the Synthesis of Protected, Primary Pentadienylamines
Connel, Richard D.,Helquist, Paul,Akermark, Bjoern
, p. 3359 - 3370 (2007/10/02)
The utility of forming N-tert-butoxycarbonyl- (Boc) and N-phthalimido-protected primary 2(E),4(E)-pentadienylamines from aldehydes and ketones is described.When diethyl -2-buten-1-yl>phosphonate (33E) is treated with s
Highly Stereoselective Route to (E)-Allyl Amines via Vinyltri-n-butylphosphonium Salts (Schweizer Reaction)
Meyers, A. I.,Lawson, Jon P.,Carver, David R.
, p. 3119 - 3123 (2007/10/02)
The reaction of vinyltri-n-butylphosphonium salts, aldehydes, and sodiophthalimide in THF gave good yields of the allylic phthalimides with high E stereoselectivity (75-100percent).The use of the vinyltriphenylphosphonium salts (Schweizer reaction) gave the allyl phthalimide with the Z isomer predominating.A study of the phthalimide cation and the effect of added lithium salt showed some reversal in the olefin geometry but in general the selectivity was only 3:1
