124754-92-3

Upstream product

• 124754-86-5 ((E)-(R)-1-Benzyloxymethyl-4-oxo-but-2-enyl)-carbamic acid tert-butyl ester 
• 79069-54-8 (S)-2-(t-butoxycarbonylamino)-3-phenylmetoxy-1-propanal 
• 92085-86-4 (+)-tert-butyl {(1R)-1-[(benzyloxy)methyl]prop-2-en-1-yl}carbamate 

Downstream Products

• 124754-55-8 (2R)-N-(tert-butoxycarbonyl)-2-amino-1-(benzyloxy)-5-chloro-3-pentene 
• 114671-11-3 (4R^*,5S^*)-4-(benzyloxymethyl)-5-vinyl-2-oxazolidinone 
• 114671-11-3 (4R^*,5R^*)-4-(benzyloxymethyl)-5-vinyl-2-oxazolidinone 
• 114671-07-7 N-(tert-butyldimethylsilyloxycarbonyl)-2-amino-1-(benzyloxy)-5-chloro-3-pentene 

Relevant academic research and scientific papers

Syntheses and reactions of silyl carbamates. 2. A new mode of cyclic carbamate formation from tert-butyldimethylsilyl carbamate

Stereoselective construction of 1,2 and 1,3 amino hydroxyl systems was achieved by the intramolecular trapping of the N-tert-butyldimethylsilyloxycarbonyl species (silyl carbamate) activated by fluoride ion. The reaction of the silyl carbamate with 1,2-sy