147688-25-3

Upstream product

• 126402-60-6 (2-{Benzyl-[4-(4,8-dimethoxy-naphthalen-1-ylmethyl)-benzenesulfonyl]-amino}-ethyl)-carbamic acid benzyl ester 
• 25711-25-5 benzyl aziridine-1-carboxylate 
• 100-46-9 benzylamine 
• 300561-17-5 N-benzyloxycarbonyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamide 
• 4152-09-4 N-benzylethylenediamine 
• 93407-96-6 2-(((benzyloxy)carbonyl)amino)ethyl 4-methylbenzenesulfonate 
• 250296-57-2 N-Benzyloxycarbonyl-N-trifluoromethylsulfonyl-4-trifluoromethylanilide 

Downstream Products

• 147688-26-4 3,9-Dibenzyl-1,11-bis(benzyloxycarbonylamino)-6-oxa-3,9-diazaundecane-4,8-dione 
• 147688-28-6 4,16-Dibenzyl-1,10-dioxa-4,7,13,16-tetraazacyclooctadecane-3,8,12,17-tetraone 
• 147688-29-7 4,16-Dibenzyl-1,10-dioxa-4,7,13,16-tetraazacyclooctadecane 
• 147688-27-5 1,11-Diamino-3,9-dibenzyl-6-oxa-3,9-diazaundecane-4,8-dione 

Relevant academic research and scientific papers

Studies on development of sufficiently chemoselective N-acylation reagents: N-Acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides

A variety of storable N-acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides (4a-e) prepared from N-2,3,4,5,6-pentafluorophenylmethanesulfonamide (3), have been developed after systematic research on the structure-reactivity relationship and were found to serve as N-acylation reagents exhibiting sufficiently good chemoselectivity. (C) 2000 Elsevier Science Ltd.

Chemoselective alkoxycarbonylation reagent having trifluoromethylsulfonyl-4-trifluoromethylanilide as a leaving group

N-Benzyloxy- and N-tert-butoxycarbonyltrifluoromethylsulfonyl-4-trifluoromethylanilides were prepared and were found to be chemoselective and shelf-storable alkoxycarbonylation reagents.

N-Benzyloxycarbonylaziridine in the Syntheses of 2-Aminoethyl Armed Lariats and Selectively N-Protected Polyazacrown Ethers

The 15- and 18-membered mono- and bi-bracchial N-aminoethylene armed lariats 6, 7 and 8 have been synthesized by alkylations of parent azacrowns using N-benzyloxycarbonylaziridine 2 and subsequent removal of Z-protecting groups by catalytic hydrogenolysis

A NEW AMINO PROTECTING GROUP READILY REMOVABLE WITH NEAR ULTRAVIOLET LIGHT AS AN APPLICATION OF ELECTRON-TRANSFER PHOTOCHEMISTRY

As an extension of organic photochemistry via intermolecular electron-transfer in donor-acceptor pair systems between electron-rich aromatic compounds and electron-deficient tosyl groups, we report here a new protecting group for the amino-function, 4-(4,8-dimethoxy-naphthylmethyl)benzenesulfonyl (DNMBS) group, which is readily removed, via an intramolecular electron-transfer followed by hydrolysis, with a high quantum efficiency on irradiation with light longer than 300 nm.