954419-90-0

Upstream product

• 421-50-1 1,1,1-trifluoro-2-propanone 
• 139278-12-9 (4S)-4-benzyl-3-<2-(triphenylphosphonio)acetyl>-2-oxazolidinone bromide 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 1027434-21-4 C₁₀H₁₃F₃O₃ 
• 1547-27-9 (E)-4,4,4-trifluoro-3-methylbut-2-enoyl chloride 
• 129549-13-9 4S-3-(2-bromoacetyl)-4-(phenylmethyl)-2-oxazolidinone 
• 400-28-2 (2E)-4,4,4-Trifluoro-3-methylbut-2-enoic acid 
• 691-77-0 (E)-3-trifluoromethyl-2-butenoic acid ethyl ester 

Downstream Products

• 952714-68-0 (S)-4-benzyl-3-((S)-4,4,4-trifluoro-3-methylbutanoyl)oxazolidin-2-one 

Relevant academic research and scientific papers

Production of chirally pure amino alcohol intermediates, derivatives thereof, and uses thereof

A method of selectively preparing a chiral 2S-amino alcohol useful in preparation of an amide sulfonated or acylated with alkyl, substituted aryl or substituted heteroaryl is described. The method involves reacting a di-tert-butyl diazene-1,2-dicarboxylat

A rapid access to both enantiomers of 1,2,3,4-tetranor B-trienic 18,18,18-trifluorosteroids. The first enantiocontrolled total synthesis of 18,18,18-trifluorosteroids

Chiral A-tetranor B-trienic 18,18,18-trifluorosteroid 2a and its enantiomer 1a were synthesised by the thermolysis of chiral olefinic benzocyclobutenes 7b and 7a which were in turn prepared by the aldol reaction of chiral oxazolidinone 5 and 11 with 2-(4-