124755-01-7

Upstream product

• 82689-16-5 benzyl {(5S)-5-[(tert-butoxycarbonyl)amino]-6-oxohexyl}carbamate 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 73548-77-3 Boc-L-Lys(Z)-OMe 
• 115384-91-3 bis(2,2,2-trifluoroethyl)(methoxy)carbonylmethylphosphonate 
• 82689-20-1 N⁶-benzyloxycarbonyl-N²-tert-butoxycarbonyl-L-lysinol 

Downstream Products

• 115384-66-2 [(S)-5-tert-Butoxycarbonylamino-5-((2R,3S)-3-hydroxymethyl-oxiranyl)-pentyl]-carbamic acid benzyl ester 
• 115384-66-2 [(S)-5-tert-Butoxycarbonylamino-5-((2S,3R)-3-hydroxymethyl-oxiranyl)-pentyl]-carbamic acid benzyl ester 
• 115384-69-5 Methanesulfonic acid (1S,2S)-6-benzyloxycarbonylamino-2-tert-butoxycarbonylamino-1-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-hexyl ester 
• 115384-70-8 (4S,5S)-4-(4-Benzyloxycarbonylamino-butyl)-5-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 115384-68-4 [(5S,6S)-5-tert-Butoxycarbonylamino-8-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-octyl]-carbamic acid benzyl ester 
• 115384-72-0 (4-{(4S,5R)-5-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-oxazolidin-4-yl}-butyl)-carbamic acid benzyl ester 
• 115384-67-3 ((5S,6S)-5-tert-Butoxycarbonylamino-6,8-dihydroxy-octyl)-carbamic acid benzyl ester 
• 115384-65-1 ((Z)-(S)-5-tert-Butoxycarbonylamino-8-hydroxy-oct-6-enyl)-carbamic acid benzyl ester 
• 124779-81-3 (4S,5R)-4-<<(N-benzyloxycarbonyl)amino>butyl>-5-vinyl-2-oxazolidinone 
• 124754-70-7 (4S,5S)-4-<<(N-benzyloxycarbonyl)amino>butyl>-5-vinyl-2-oxazolidinone 
• 124754-58-1 C₂₃H₃₇ClN₂O₄Si 
• 124754-56-9 (4S)-N⁸-(benzyloxycarbonyl)-N⁴-(tert-butoxycarbonyl)-4,8-diamino-1-chloro-2-octene 
• 1026029-45-7 (E)-(S)-8-Benzyloxycarbonylamino-4-[3-(2-iodo-phenyl)-ureido]-oct-2-enoic acid methyl ester 

Relevant academic research and scientific papers

A novel synthesis of 1,3-benzodiazepin-2-ones using intramolecular heck reaction

The formation of the skeleton of 1,3-benzodiazepin-2-one could be efficiently achieved by intramolecular Heck reaction. This methodology was well applicable to the preparation of optically pure 4-substituted 1,3-benzodiazepin-2-ones starting from easily available α-amino acids.

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

Synthesis and Absolute Structure of Galantinamic Acid

The structure of galantinamic acid (2) has been confirmed to be (2R,3S,5S,6R)-25 by the stereoselective synthesis of each of the eight diastereomers derived from L-lysine; total synthesis of the natural form was accomplished by starting from D-lysine