88818-16-0

Upstream product

• 3426-71-9 Benzyl N-hydroxycarbamate 

Downstream Products

• 94936-55-7 methyl 3-benzyloxycarbonyl-2-oxa-3,5-diazabicyclo<2.2.2>oct-7-ene-5-carboxylate 
• 94936-50-2 (1S,4R)-3-Oxa-2,5-diaza-bicyclo[2.2.2]oct-7-ene-2,5-dicarboxylic acid 2-benzyl ester 5-methyl ester 
• 102115-94-6 3-benzyloxycarbonyl-2-oxa-3-azabicyclo<2.2.2>oct-5-ene-1-carbonitrile 
• 96657-42-0 ethyl 3-benzyloxycarbonyl-2-oxa-3-azabicyclo<2.2.2>oct-5-ene-1-carboxylate 
• 110261-69-3 benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate 
• 110261-62-6 benzyl trans-6-(dimethoxymethyl)-3,6-dihydro-3-methyl-2H-1,2-oxazine-2-carboxylate 
• 110261-62-6 benzyl cis-6-(dimethoxymethyl)-3,6-dihydro-3-methyl-2H-1,2-oxazine-2-carboxylate 
• 1318768-16-9 benzyl (2-(pyridin-2-yl)phenyl)carbamate 
• 114217-88-8 methyl 3-benzyloxycarbonyl-7,8-diacetoxy-2-oxa-3,5-diazabicyclo<2.2.2>octane-5-carboxylate 
• 114217-87-7 methyl 2-benzyloxycarbonyl-7,8-diacetoxy-3-oxa-2,5-diazabicyclo<2.2.2>octane-5-carboxylate 
• 94936-29-5 methyl 3-benzyloxycarbonyl-7,8-dihydroxy-2-oxa-3,5-diazabicyclo<2.2.2>octane-5-carboxylate 
• 94936-26-2 methyl 2-benzyloxycarbonyl-7,8-dihydroxy-3-oxa-2,5-diazabicyclo<2.2.2>octane-5-carboxylate 
• 102115-95-7 3-benzyloxycarbonyl-1-<<(tert-butoxycarbonyl)amino>methyl>-2-oxa-3-azabicyclo<2.2.2>oct-5-ene 
• 88818-05-7 3-benzyloxycarbonyl-2-oxa-3-azabicyclo<2.2.2>oct-5-ene-1-methanol 

Relevant academic research and scientific papers

Rh(III)-Catalyzed C-H amidation with N-Hydroxycarbamates: A new entry to N-Carbamate-protected arylamines

An unprecedented Rh(III)-catalyzed direct intermolecular C-H amidation with N-hydroxycarbamates has been developed. Different directing groups, such as pyridine, pyrimidine, pyrazole, and N-OMe oxime, can be employed in this C-H amidation process, providi

The electrophilic α-amination of α-alkyl-β-ketoesters with in situ generated nitrosoformates

Lewis acid and oxidation catalysis are merged in the reaction discussed here, which provides access to diversely substituted N-hydroxycarbamates (see scheme). This reaction highlights the potential of nitrosoformates as electrophilic amination reagents as

SYNTHESIS OF RACEMIC DIAMINO-DIDEOXY-LYXOPYRANOSE DERIVATIVES USING ACILNITROSO DIENOPHILES (1).

Acylnitroso derivatives, which are obtained by in situ oxidation of the corresponding hydroxamic acids with tetraalkylammonium iodate, react intantaneously in the presence of dihydropyridine 1 leading to the Diels-Alder adducts 4 and 5.These latter ones w