732284-14-9Relevant academic research and scientific papers
Highly Regio- and Stereoselective Ni-Catalyzed Hydrocyanation of 1,3-Enynes
Sun, Feilong,Ni, Jie,Cheng, Gui-Juan,Fang, Xianjie
, p. 5956 - 5960 (2020)
A highly regio- and stereoselective hydrocyanation of 1,3-enynes was implemented by nickel/diphosphine catalysts. A wide range of highly regio- and stereoselective alkenyl nitriles were efficiently prepared. In this transformation, both the tethered alken
Convenient synthetic route to an enantiomerically pure FMOC α-amino acid
Taber, Douglass F.,Berry, James F.,Martin, Timothy J.
supporting information; experimental part, p. 9334 - 9339 (2009/04/06)
(Chemical Equation Presented) A strategy for the facile α-amination of carboxylic acid menthyl esters is described. The resulting diastereomers, readily separable, can be individually carried on to each enantiomer of the FMOC α-amino acid. A variety of un
Gold catalysis: Mild conditions for the transformation of alkynyl epoxides to furans
Stephen,Hashmi,Sinha, Pradipta
, p. 432 - 438 (2007/10/03)
GoLd(III) chloride catalyzes the isomerization of alkynyl epoxides to furans under mild conditions. Additional functional groups like hydroxy groups or aryl bromides do not need to be protected.
