26903-66-2

Upstream product

• 1026206-49-4 2-chloromethyl-2-isopropyloxirane 
• 50-00-0 formaldehyd 
• 55023-48-8 1-(3-methyl-but-1-enyl)-pyrrolidine 
• 563-78-0 2,3-Dimethyl-1-butene 

Downstream Products

• 148675-55-2 1-(4-methoxybenzyloxy)-2-(2-propyl)-2-propene 
• 65860-53-9 2-isopropyl-3-butenoic acid 
• 38972-59-7 trans-3,4-dimethyl-2-pentenoic acid 
• 49642-48-0 2,3-dimethylbutanal 
• 1415357-62-8 C₁₄H₁₆O₂ 
• 1601490-29-2 (R)-2-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-7-fluoro-4-isopropyl-2,3,4,5-tetrahydrobenzo[1,2-f]thiazepine 1,1-dioxide 
• 1601490-24-7 (S)-2-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-7-fluoro-4-isopropyl-2,3,4,5-tetrahydrobenzo[1,2-f]thiazepine 1,1-dioxide 
• 1601490-09-8 2-bromo-4-fluoro-N-(3-methyl-2-methylenebutyl)benzenesulfonamide 
• 1601490-02-1 2-bromo-4-fluoro-N-(4-methoxybenzyl)-N-(3-methyl-2-methylenebutyl)benzenesulfonamide 
• 1601490-36-1 (S)-tetrahydrofuran-3-yl ((2S,3R)-4-((S)-7-fluoro-4-isopropyl-1,1-dioxido-4,5-dihydrobenzo[1,2-f]thiazepin-2(3H)-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamate 
• 1601490-32-7 (S)-tetrahydrofuran-3-yl ((2S,3R)-4-((R)-7-fluoro-4-isopropyl-1,1-dioxido-4,5-dihydrobenzo[1,2-f]thiazepin-2(3H)-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamate 
• 1601490-35-0 1-(tert-butyl)-3-((2S,3R)-4-((R)-7-fluoro-4-isopropyl-1,1-dioxido-4,5-dihydrobenzo[1,2-f]thiazepin-2(3H)-yl)-3-hydroxy-1-phenylbutan-2-yl)urea 
• 1601490-19-0 tert-butyl ((2S,3R)-4-((R)-7-fluoro-4-isopropyl-1,1-dioxido-4,5-dihydrobenzo[1,2-f]thiazepin-2(3H)-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamate 
• 1357179-55-5 3-methyl-2-methylenebutyl 4-methylbenzenesulfonate 

Relevant academic research and scientific papers

Direct enantioselective organocatalytic hydroxymethylation of aldehydes catalyzed by α,α-diphenylprolinol trimethylsilyl ether

The direct enantioselective hydroxymethylation of aldehydes utilizing α,α-diphenylprolinol trimethylsilyl ether as an organocatalyst is described. The intermediate α-substituted β-hydroxyaldehydes were not isolated but converted to the more readily isolab

Reactions of 2-substituted epichlorohydrins

2-Substituted epichlorohydrins have been synthesized by starting with 1,2-dichloro acetone and various alkyl and aryl halides via dichlorohydrins followed by cyclization. The reactive 2-substituted epichlorohydrins were subjected to nucleophilic attacking of azide and cyanide ions to afford corresponding β-azido alcohols and α,β-unsaturated nitriles.