799559-97-0

Upstream product

• 108-98-5 thiophenol 
• 799559-79-8 (S)-[(S)-1-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyl]oxirane 
• 440083-43-2 (2S,3S)-6-(tert-butyldimethylsilyl)oxy-2,3-epoxyhexan-1-ol 
• 1041927-30-3 (2S,3S)-3-Azido-6-(tert-butyl-dimethyl-silanyloxy)-hexane-1,2-diol 
• 799560-51-3 [4-(tert-butyl-dimethyl-silanyloxy)-1-(1,2-dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester 
• 98897-64-4 (E)-6-[(tert-butyldimethylsilyl)oxy]-2-hexen-1-ol 

Downstream Products

• 799560-37-5 (2S,3S)-3-(tert-butoxycarbonylamino)-6-(tert-butyldimethylsilyloxy)-1-phenylsulfonyl-2-hexanol 

Relevant academic research and scientific papers

Enantiodivergent, catalytic asymmetric synthesis of γ-amino vinyl sulfones

A set of diversely substituted N-Boc-γ-amino vinyl sulfones has been prepared by a four-step procedure from readily available, highly enantiopure anti-N-Boc-3-amino-1,2-alkanediols. This new route, which does not depend on the accessibility of α-amino acids as starting materials, is noteworthy for its efficiency, for its generality, and for the fact that both enantiomers of a given γ-amino vinyl sulfone can be obtained with equal ease.