414858-85-8

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 65275-66-3 methyl α-(phenylseleno)propionate 

Downstream Products

• 204202-29-9 (2R,3S,4S)-5-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2,4-dimethyl-pentanoic acid methyl ester 
• 367264-31-1 (2S,3R,4S)-5-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2,4-dimethyl-pentanoic acid methyl ester 
• 367264-63-9 (2R,3R,4S)-5-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2,4-dimethyl-pentanoic acid methyl ester 
• 367264-21-9 (2R,3R,4S)-4-benzyloxy-3-hydroxy-2-methyl-2-phenylselanyl-pentanoic acid methyl ester 
• 94989-84-1 (2S,3S,4S)-4-benzyloxy-3-hydroxy-2-methyl-pentanoic acid methyl ester 
• 95043-91-7 (2R,3S,4S)-4-benzyloxy-3-hydroxy-2-methyl-pentanoic acid methyl ester 

Relevant academic research and scientific papers

Enantioselective synthesis of the optically active α-methylene- β-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization

The asymmetric aldol reaction of a tetra-substituted ketene silyl acetal including an alkylseleno group with aldehydes has been developed by the promotion of Sn(OTf)2 coordinated with a chiral diamine to afford the corresponding aldols having c