Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Anudeep Kumar Narula"'
Autor:
Ashmita Singh, Anudeep Kumar Narula
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100279- (2022)
A new and facile methodology was developed for the synthesis of a wide variety of synthetically important propargylamines via the A3 coupling reaction of aryl aldehydes, phenyl acetylenes, and amines. The reaction was catalyzed by tetra-butyl ammoniu
Externí odkaz:
https://doaj.org/article/d1023a1b8d0946ecb1dcf87a3363a96a
Publikováno v:
Journal of Heterocyclic Chemistry. 59:2037-2046
Autor:
Ashmita Singh, Anudeep Kumar Narula
Publikováno v:
ChemistrySelect. 6:7794-7798
Autor:
Anudeep Kumar Narula, Preeti Sehgal
Publikováno v:
Journal of Materials Science: Materials in Electronics. 32:16612-16622
The double composite layer composed of europium and terbium doped zinc oxide (Eu3+,Tb3+@ZnO) as downconversion material (DC) and neodymium and ytterbium-doped zinc oxide (Nd3+,Yb3+@ZnO) as upconversion materials (UC) was prepared and used as photoano
Publikováno v:
Chinese Journal of Chemistry. 39:1503-1510
Autor:
Anudeep Kumar Narula, Ashmita Singh
Publikováno v:
New Journal of Chemistry. 45:7486-7490
A facile method for the amidation of aldehydes by a cascade approach was developed. This methodology, reported for the first time, uses a N-heterocyclic carbene (NHC) as the catalyst, and N-hydroxysuccinimide (NHS) mediated synthesis of amides utilis
Autor:
Ashmita Singh, Anudeep Kumar Narula
Publikováno v:
Synlett. 32:718-722
A one-pot two-step oxidative process has been developed for the tert-butyl hydroperoxide mediated transformation of aldehydes and amines into amides catalyzed by copper(I) iodide and an N-heterocyclic carbene. The process is additive-free and does no
Publikováno v:
ChemistrySelect. 5:9417-9423
Autor:
Tapasya Srivastava, Divyank Mahajan, Mansi Pandit, Deepa Deswal, Anudeep Kumar Narula, N. Latha, Pratibha Shukla
Publikováno v:
Drug development researchREFERENCES. 83(2)
New candidates of imidazo [1, 2-a] pyridine were designed by combining 2-amino pyridine, TOSMIC isocyanide and various assorted aldehydes were synthesized to explore their antioxidant and antifungal potential. The design of these derivatives was base
Publikováno v:
Future Medicinal Chemistry. 11:2663-2686
Aim: The global burden of fungal infections has transitioned from a case–specific observation to a major cause of high human mortality. Therefore, novel compounds with innovative methodologies need to be synthesized and evaluated for their antifung