Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Laxmi Deswal"'
Autor:
Laxmi Deswal, Vikas Verma, Jagat Singh Kirar, Devinder Kumar, Yogesh Deswal, Ashwani Kumar, Meenakshi Bhatia
Publikováno v:
Research on Chemical Intermediates. 49:1059-1083
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b1394660bc34a9a7af9cf25103bc23f
https://doi.org/10.1007/s11164-022-04921-4
https://doi.org/10.1007/s11164-022-04921-4
Autor:
Laxmi Deswal, Vikas Verma, Devinder Kumar, Yogesh Deswal, Ashwani Kumar, Rajnish Kumar, Mahavir Parshad, Meenakshi Bhatia
Publikováno v:
Chemical Papers. 76:7607-7622
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2e51218caf7a21e275e7604a2ee57ba
https://doi.org/10.1007/s11696-022-02436-1
https://doi.org/10.1007/s11696-022-02436-1
Autor:
Yogesh Deswal, Sonika Asija, Aisha Tufail, Amit Dubey, Laxmi Deswal, Naresh Kumar, Sonia Saroya, Jagat Singh Kirar, Neeraj Mohan Gupta
Publikováno v:
Applied Organometallic Chemistry. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c2483261642b9069a677c333102e355
https://doi.org/10.1002/aoc.7050
https://doi.org/10.1002/aoc.7050
Publikováno v:
Synthetic Communications. 51:2832-2846
The present study describes a facile and efficient synthesis of 1-(N-arylacetamide)-4-phenyl-2-pyrazolyl-imidazole 7a–7t by reacting 1-(4-phenyl-1H-imidazol-2-yl)-1H-pyrazole (3a)/3,5-dimethyl-1-(4-phenyl-1H-imidazol-2-yl)-1H-pyrazole (3b) with 2-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f89726f1c7751976733e57ae8adac29
https://doi.org/10.1080/00397911.2021.1953532
https://doi.org/10.1080/00397911.2021.1953532
Autor:
Suman Punia, Vikas Verma, Devinder Kumar, Ashwani Kumar, Laxmi Deswal, Gurjaspreet Singh, Subhash C. Sahoo
Publikováno v:
Journal of Molecular Structure. 1262:133060
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d773693b9a9a8f0002e8287a9c52088c
https://doi.org/10.1016/j.molstruc.2022.133060
https://doi.org/10.1016/j.molstruc.2022.133060
Autor:
Laxmi Deswal, Meenakshi Bhatia, Yogesh Deswal, Vikas Verma, Ashwani Kumar, Anil Kumar, Devinder Kumar
Publikováno v:
Future medicinal chemistry. 13(11)
Background: Considering emerging drug resistance in microbes, this work is focused on the synthesis of azole hybrids as novel antimicrobials. Materials & methods: The triazole derivatives were prepared using azide alkyne cycloaddition reaction. The a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c14270f263ab035e9332c20eccf214
https://pubmed.ncbi.nlm.nih.gov/33896215
https://pubmed.ncbi.nlm.nih.gov/33896215
Autor:
Yogesh Deswal, Sonika Asija, Amit Dubey, Laxmi Deswal, Deepak Kumar, Deepak Kumar Jindal, Jai Devi
Publikováno v:
Journal of Molecular Structure. 1253:132266
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa814052fea55dfae05af73388174671
https://doi.org/10.1016/j.molstruc.2021.132266
https://doi.org/10.1016/j.molstruc.2021.132266
Publikováno v:
Journal of Molecular Structure. 1223:129216
A series of eighteen pyrazole-imidazole-triazole hybrid (2-(4-((2-(substituted-1H-pyrazol-1-yl)-4-phenyl-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)-N-(substituted)phenylacetami- de) (6a-6r) are synthesized through click reaction between in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c98162f3a6eb370ecc09ae94296fc612
https://doi.org/10.1016/j.molstruc.2020.129216
https://doi.org/10.1016/j.molstruc.2020.129216
Autor:
C. P. Kaushik, Suman Punia, Devinder Kumar, Yogesh Deswal, Vikas Verma, Ashwani Kumar, Laxmi Deswal
Publikováno v:
Archiv der Pharmazie. 353:2000090
Some novel benzimidazole-tethered 1,2,3-triazole derivatives (4a-r) were synthesized by a click reaction between 2-substituted 1-(prop-2-yn-1-yl)-1H-benzo[d]imidazole and in situ azide. The structures of the synthesized compounds were confirmed by sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d9e2ff5d8eac84dbae6a97f74092c11
https://doi.org/10.1002/ardp.202000090
https://doi.org/10.1002/ardp.202000090