1073166-62-7Relevant academic research and scientific papers
Enantioselective epoxidation of α,β-enones promoted by (1R,3S,4S)-2-azanorbornyl-3-methanol as an organocatalyst
Lu, Jun,Xu, Yun-He,Liu, Feng,Loh, Teck-Peng
, p. 6007 - 6008 (2008)
(1R,3S,4S)-2-Azanorbornyl-3-methanol was synthesized form (R)-1-phenylethylamine and used as a catalyst for the enantioselective epoxidation of α,β-enones to afford the corresponding epoxides in good yields and high enantioselectivities at room temperature.
Aldol reaction under solvent-free conditions: Highly stereoselective synthesis of 1,3-amino alcohols
Loh, Teck-Peng,Huang, Jing-Mei,Goh, Swee-Hock,Vittal, Jagadese J.
, p. 1291 - 1294 (2007/10/03)
(formula presented) A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity obs
Asymmetric aza-diels-alder reaction using the chiral 1-phenyl ethyl imine of methyl glyoxylate
Stella,Abraham,Feneau-Dupont,Tinant,Declercq
, p. 2603 - 2606 (2007/10/02)
The Diels-Alder reaction between cyclopentadiene and the chiral 1-phenyl-ethyl imine of methyl glyoxylate takes place very easily by activation with trifluoroacetic acid and boron trifluoride etherate to provide diastereoselectively (total face selectivit
