143950-29-2

Upstream product

• 50629-48-6 2-trimethylsilyloxy-3,4-dihydronaphthalene 
• 144016-22-8 (2S,4R,5R)-2-methoxy-4-methyl-3-(4-methylbenzenesulfonyl)-5-phenyl-1,3-oxazolidine 
• 98-59-9 p-toluenesulfonyl chloride 
• 53643-20-2 (1R,2R)-norephedrine hydrochloride 
• 143957-01-1 (1'R,2'R)-N-(2-hydroxy-1-methyl-2-phenylethyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Origins of aryl substituent effects on the stereoselectivities of additions of silyl enol ethers to a chiral oxazolinium ion

Density functional theory calculations are reported that reveal the role of aromatic interactions in the additions of aryl-substituted silyl enol ethers to a chiral oxazolinium ion. Aryl-substituted silyl enol ethers give the opposite diastereomer of the

Norpseudoephedrine-derived 2-methoxy-2-sulfonyl-1,3-oxazolidines: Chiral, highly diastereoselective formyl cation equivalents

(2S,4R,5R)-2-Methoxy-4-methyl-3-(4-methylbenzenesulfonyl)-5- phenyl-1,3-oxazolidine (2c) adds trimethylsilyl 1-cycloalkenyl ethers under Lewis acid catalysis with complete induced and high simple diastereoselectivity to yield homichiral oxazolidine-masked