119969-33-4Relevant academic research and scientific papers
Enantioselective ring-opening reactions of racemic ethynyl epoxides via copper-allenylidene intermediates: Efficient approach to chiral β-amino alcohols
Hattori, Gaku,Yoshida, Akiko,Miyake, Yoshihiro,Nishibayashi, Yoshiaki
experimental part, p. 7603 - 7607 (2009/12/24)
(Chemical Equation Presented) Enantioselective copper-catalyzed ring-opening reactions of racemic ethynyl epoxides with amines using (R)-DTBM-MeO-BIPHEP as a chiral ligand have been found to give the corresponding amino alcohols in high yields with up to
SUBSTITUTED FURANS AS INHIBITORS OF 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE
-
, (2008/06/13)
Compounds of the formula: STR1 in which STR2 where M is hydrogen or alkyl; one of R 2 and R 3 is phenyl or substituted phenyl where the substituent is alkyl, alkoxy, halogen, trifluoromethyl, nitro, amino, cyano or carboxyl; and the other
