745794-13-2

Upstream product

• 903907-75-5 (R)-tert-butyl 4-((S)-1-((benzyloxycarbonyl)(4-methoxybenzyl)amino)but-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 745794-12-1 (R)-tert-butyl-4-((S)-1-(4-methoxybenzylamino)but-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 745794-10-9 (R)-4-{(S)-1-[Hydroxy-(4-methoxy-benzyl)-amino]-but-3-enyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 745794-09-6 (Z)-N-[(4R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-1,3-oxazolidin-4-ylidene]-4-methoxybenzylamine N-oxide 
• 501-53-1 benzyl chloroformate 
• 108149-63-9 4-hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 102308-32-7 (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 745794-08-5 {(1R,2S)-2-[Benzyloxycarbonyl-(4-methoxy-benzyl)-amino]-1-hydroxymethyl-pent-4-enyl}-carbamic acid tert-butyl ester 

Downstream Products

• 745794-14-3 [(1R,2S)-2-[Benzyloxycarbonyl-(4-methoxy-benzyl)-amino]-1-(1-hydroxy-allyl)-pent-4-enyl]-carbamic acid tert-butyl ester 
• 745794-20-1 (4S,5S,2E)-ethyl 5-[benzyloxycarbonyl-(4-methoxybenzyl)amino]-4-(tert-butoxycarbonylamino)octa-2,7-dienate 
• 745794-23-4 (1R,5S,6R,7R)-[7-hydroxy-4-(4-methoxybenzyl)-3-oxo-2-oxa-4-azabicyclo[3.2.1]oct-6-yl]carbamic acid tert-butyl ester 
• 745794-07-4 (1S,5S)-{5-[benzyloxycarbonyl-(4-methoxybenzyl)amino]cyclopent-2-enyl}carbamic acid tert-butyl ester 
• 745794-06-3 (1R,2R,6S)-{6-[benzyloxycarbonyl-(4-methoxybenzyl)amino]-2-hydroxycyclohex-3-enyl}carbamic acid tert-butyl ester 
• 745794-22-3 (1R,2R,3S,5S)-{3-[benzyloxycarbonyl-(4-methoxybenzyl)amino]-6-oxabicyclo[3.1.0]hex-2-yl}carbamic acid tert-butyl ester 
• 745794-18-7 (1S,2S,3R,4S,6R)-{4-[benzyloxycarbonyl-(4-methoxybenzyl)amino]-2-hydroxy-7-oxabicyclo[4.1.0]hept-3-yl}carbamic acid tert-butyl ester 
• 745794-19-8 (1R,2S,3R,4S,6S)-{6-[benzyloxycarbonyl-(4-methoxybenzyl)amino]-2,3,4-trihydroxycyclohexyl}carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

RCM approaches toward the diastereoselective synthesis of vicinal trans-diaminocyclitols from L-serine

Starting from L-serine, the asymmetric synthesis of four diaminocyclitol derivatives as sugar-based glycosidase inhibitors has been achieved using ring-closing metathesis (RCM) as a key step. Introduction of vicinal trans-diamino functionality onto the ac