Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pramod S. Mali"'
Publikováno v:
Analytical Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca4eafdeea759c5bcfbd5a7cc5ccb421
https://doi.org/10.1021/acs.analchem.2c05485
https://doi.org/10.1021/acs.analchem.2c05485
Autor:
Mohammad Mehdi Ghanbarnezhad, Mohammad Bagher Shahsavani, Pramod S. Mali, Mansi Upadhyay, Ashutosh Kumar, Rawayh Muslim Albaghlani, Ali Niazi, Reza Yousefi
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1866:130150
Among the various treatments, GLP-1 receptor agonists (incretin mimics) such as liraglutide and exenatide have been well received in treating type 2 diabetes mellitus (T2DM) and obesity. In this study, an exenatide analogue, in which methionine at po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c445f41f28a126caa1972c6a5e395cb6
https://doi.org/10.1016/j.bbagen.2022.130150
https://doi.org/10.1016/j.bbagen.2022.130150
Publikováno v:
Synthesis. 49:5224-5230
Tf2NH-catalyzed tandem 1,6-conjugate addition/Schmidt type rearrangement using vinyl azides and p-quinone methides to access a variety of β-bis-arylated amides is reported. The method is quick, efficient, mild, and high yielding with broad substrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2146a72e213b950ddd64192431af296f
https://doi.org/10.1055/s-0036-1588546
https://doi.org/10.1055/s-0036-1588546
Publikováno v:
Journal of Chemical Sciences. 129:1143-1152
Synthesis of meta-substituted phosphinite ligands 3,3 $$'$$ -(methoxyphosphanediyl)bis(N,N- diethylaniline) (4a) and methoxybis(3-methoxyphenyl)phosphane (4b), in high yields, has been demonstrated. Typical phosphorus chemical shift between 110–120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b1b00e980304ae22b56f560f5c91801
https://doi.org/10.1007/s12039-017-1341-z
https://doi.org/10.1007/s12039-017-1341-z
Publikováno v:
Organic letters. 19(12)
A method for the cross-coupling reactions of aryldiazonium salts with trialkylallylsilanes via merged gold/photoredox catalysis is described. The reaction is proposed to proceed through a photoredox-promoted generation of an electrophilic arylgold(II
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5228015a39dcbd43d2e76482943a4d16
https://pubmed.ncbi.nlm.nih.gov/28590758
https://pubmed.ncbi.nlm.nih.gov/28590758