Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Manoj Kumar Gangwar"'
Autor:
Abeer Nasser Al-Romaizan, Manoj Kumar Gangwar, Ankit Verma, Salem M. Bawaked, Tamer S. Saleh, Rahmah H. Al-Ammari, Ray J. Butcher, Ibadur Rahman Siddiqui, Mohamed Mokhtar M. Mostafa
Publikováno v:
Molecules, Vol 28, Iss 13, p 4992 (2023)
For the creation of adaptable carbonyl compounds in organic synthesis, the oxidation of alcohols is a crucial step. As a sustainable alternative to the harmful traditional oxidation processes, transition-metal catalysts have recently attracted a lot
Externí odkaz:
https://doaj.org/article/9d75e436d74343da90b91316dd3a19a0
Publikováno v:
ACS Omega, Vol 3, Iss 2, Pp 1740-1756 (2018)
Externí odkaz:
https://doaj.org/article/5ab8180c8382485c8b615717f354d3e4
Publikováno v:
ACS Omega, Vol 2, Iss 8, Pp 4737-4750 (2017)
Externí odkaz:
https://doaj.org/article/e17da0ec0364448bb07c6903aa27ece9
Autor:
Anuj Kumar, Afsana Naaz, A. P. Prakasham, Manoj Kumar Gangwar, Raymond J. Butcher, Dulal Panda, Prasenjit Ghosh
Publikováno v:
ACS Omega, Vol 2, Iss 8, Pp 4632-4646 (2017)
Externí odkaz:
https://doaj.org/article/319ab9e7c4934aa69d109e0ecaec2820
Autor:
Manoj Kumar Gangwar, Swechchha Pandey, Rajesh Kumar Parsapur, Moussab Harb, Sathiyamoorthy Murugesan, Abdul-Hamid Emwas, Omer Refa Koseoglu, Robert Peter Hodgkins, Anissa Bendjeriou-Sedjerari, Magnus Rueping, Kuo-Wei Huang, Jean-Marie Basset
Publikováno v:
Chemistry of Materials. 34:8777-8789
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1cedea09f4e98570e4d766812bfd229
https://doi.org/10.1021/acs.chemmater.2c02033
https://doi.org/10.1021/acs.chemmater.2c02033
Autor:
Mostafa, Abeer Nasser Al-Romaizan, Manoj Kumar Gangwar, Ankit Verma, Salem M. Bawaked, Tamer S. Saleh, Rahmah H. Al-Ammari, Ray J. Butcher, Ibadur Rahman Siddiqui, Mohamed Mokhtar M.
Publikováno v:
Molecules; Volume 28; Issue 13; Pages: 4992
For the creation of adaptable carbonyl compounds in organic synthesis, the oxidation of alcohols is a crucial step. As a sustainable alternative to the harmful traditional oxidation processes, transition-metal catalysts have recently attracted a lot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::624797242a0a83f224ba70501133ceb1
Publikováno v:
Asian Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62a1ca1bc510ab3db6242be1a4c50a2a
https://doi.org/10.1002/ajoc.202300085
https://doi.org/10.1002/ajoc.202300085
Autor:
Ashfaq Ahmad, Himangsu Sekhar Dutta, Mohit Kumar, null Raziullah, Manoj Kumar Gangwar, Dipankar Koley
Publikováno v:
Organic Letters. 24:2783-2787
A palladium catalyzed directing group assisted cross-coupling of aliphatic aziridines with indole, indoline, tetrahydroquinoline, and aniline has been developed to furnish the corresponding β-arylethylamine derivatives. The substrate scope was very
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e0dae211b13ed4522a072de3c690215
https://doi.org/10.1021/acs.orglett.2c00120
https://doi.org/10.1021/acs.orglett.2c00120
Autor:
null Raziullah, Mohit Kumar, Ashfaq Ahmad, Himangsu Sekhar Dutta, Anushka Rastogi, Manoj Kumar Gangwar, Dipankar Koley
Publikováno v:
Chemical Communications. 58:3481-3484
A method to functionalize the arene ring of pirfenidone has been demonstrated using pyridone as a directing group. Unlike the functionalization of the pyridone nucleus, the method demonstrated here is the alkenylation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb4b68571fc1e40c12535533f052a917
https://doi.org/10.1039/d2cc00257d
https://doi.org/10.1039/d2cc00257d
Autor:
Manoj Kumar Gangwar, Dipankar Koley, Ashfaq Ahmad, Raziullah, Ravi Sankar Ampapathi, Afsar Ali Khan, Himangsu Sekhar Dutta, Mohit Kumar, Jayanti Vaishnav
Publikováno v:
The Journal of Organic Chemistry. 86:16558-16572
A ytterbium triflate-catalyzed diastereoselective [3 + 2] cycloaddition of quinoxalinones with donor-acceptor cyclopropanes and cyclobutanes is described. A series of tetrahydropyrrolo-quinoxalinone derivatives were obtained in high yields (up to 96%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fc098e83378b1680f61b2c3f99724ea
https://doi.org/10.1021/acs.joc.1c01872
https://doi.org/10.1021/acs.joc.1c01872