5819-21-6Relevant articles and documents
Selective modification of streptozotocin at the C3 position to improve its bioactivity as antibiotic and reduce its cytotoxicity towards insulin-producing β cells
Minnaard, Adriaan J.,Walvoort, Marthe T. C.,Witte, Martin D.,Yakovlieva, Liubov,Zhang, Ji,de Haan, Bart J.,de Vos, Paul
, (2020/04/28)
With the increasing resistance of bacteria to current antibiotics, novel compounds are urgently needed to treat bacterial infections. Streptozotocin (STZ) is a natural product that has broad-spectrum antibiotic activity, albeit with limited use because of
Transesterification of alkyl carbamate to aryl carbamate : Effect of varying the alkyl group
Deshpande, Sunita R.,Likhite, Anjali P.,Rajappa, Srinivasachari
, p. 10367 - 10370 (2007/10/02)
Phosphorus oxychloride mediated transesterification of four alkyl N-methylcarbamates to several aryl N-methylcarbamates has been studied. Best yields are obtained from benzyl N-methylcarbamate.
A non-MIC route to carbamates: Irreversible trans-esterification reaction of methyl N-methylcarbamate with phenolic substrates possessing additional functional groups
Kumaran, G.,Naik, R. H.,Kulkarni, G. H.
, p. 893 - 895 (2007/10/02)
The novel non-MIC route to aryl carbamates, involving irreversible trans-esterification of methyl N-methylcarbamate has been carried out on a variety of phenolic substrates possessing additional functional groups for studying the scope of the reaction.The carbamates, thus synthesised, have been screened for their insecticidal activity against Musca domestica.