903907-79-9

Upstream product

• 152491-85-5 (R)-[1-(tert-butyl-dimethyl-silanyloxymethyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester 
• 903907-78-8 tert-butyl (4R)-4-((5S)-7-hydroxy-11,11-dimethyl-3-oxo-1,10,10-triphenyl-2,9-dioxa-4-aza-10-siladodecan-5-yl)-2,2-dimethyloxazolidine-3-carboxylate 
• 903907-77-7 (4R)-((1S)-benzyloxycarbonylamino-3,4-dihydroxybutyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 140200-05-1 tert-butyl (S)-1-(tert-butyldimethylsilyloxy)-3-oxopropan-2-yl carbamate 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 903907-85-7 [(1R,2S)-2-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-1-((R)-1-methoxymethoxy-allyl)-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-82-4 [(2R)-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-(1R)-((1S)-hydroxy-allyl)-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-81-3 [(2R)-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-(1R)-((1R)-hydroxy-allyl)-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-86-8 [(1R,2R,6S)-6-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-2-methoxymethoxy-cyclohex-3-enyl]carbamic acid tert-butyl ester 
• 903907-89-1 (3R,4R,5S)-5-benzyloxycarbonylamino-4-tert-butyloxycarbonylamino-3-methoxymethoxy-cyclohex-1-enecarboxylic acid ethyl ester 
• 903907-88-0 (3R,4R,5S)-5-Benzyloxycarbonylamino-4-tert-butoxycarbonylamino-3-methoxymethoxy-cyclohex-1-enecarboxylic acid 
• 903907-87-9 ((1S,5R,6R)-6-tert-butyloxycarbonylamino-3-hydroxymethyl-5-methoxymethoxy-cyclohex-3-enyl)carbamic acid benzyl ester 
• 903907-90-4 (3R,4R,5S)-4-acetylamino-5-benzyloxycarbonylamino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester 
• 903907-74-4 (3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester 
• 903907-80-2 [(2S)-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-(1R)-hydroxymethyl-pent-4-enyl]carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of syn-vicinal diamines via the stereoselective allylation of acyclic chiral α-amino aldimines

The stereoselective allylation of acyclic chiral α-amino aldimines affording vicinal diamines, mediated by various Lewis acids (TiCl4, SnCl4, MgBr2·OEt2, BF3·OEt2, ZnCl2), is des

Ring-closing metathesis-based synthesis of (3R,4R,5S)-4-acetylamino-5- amino-3-hydroxy-cyclohex-1-ene-carboxylic acid ethyl ester: A functionalized cycloalkene skeleton of GS4104

(3R,4R,5S)-4-Acetylamino-5-amino-3-hydroxy-cyclohex-1-ene-carboxylic acid ethyl ester, a functionalized cyclohexene skeleton of GS4104, was diastereoselectively synthesized. A major advantage of this synthesis is the use of readily available L-serine to r