Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Abhay S. Zambare"'
Publikováno v:
RSC advances. 9(41)
This work investigated a novel nonpetroleum-based catalytic process of methanol to phenol. The idea was to convert methanol to produce a main product stream having a molar ratio of propylene to benzene/toluene of unity along with relatively higher-va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1deb9aef4ebd9231940e9c562ee93a0f
https://pubmed.ncbi.nlm.nih.gov/35530611
https://pubmed.ncbi.nlm.nih.gov/35530611
Autor:
Abhay S. Zambare, Jaiprakash N. Sangshetti, Sureshchandra P. Zambare, Shantanu D. Shinde, Firoz A. Kalam Khan
Publikováno v:
Current Organic Chemistry. 20:798-828
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13edec44d7bc7e4777e2cf4eed9ac685
https://doi.org/10.2174/1385272820666151026224227
https://doi.org/10.2174/1385272820666151026224227
Autor:
Firoz A. Kalam Khan, Abhay S. Zambare, Jaiprakash N. Sangshetti, Zahid Zaheer, Indrajeet D. Gonjari
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 14:988-1020
4,5,6,7-Tetrahydrothieno pyridine is an important class of heterocyclic nucleus. Various 4,5,6,7-tetrahydrothieno pyridine derivatives have been synthesized and evaluated for various biological activities in different models with desired findings. So
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::522b514eb83317b2eb834de43a552cba
https://doi.org/10.2174/1389557514666141106131425
https://doi.org/10.2174/1389557514666141106131425
Publikováno v:
Mini-Reviews in Organic Chemistry. 11:225-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb6ac2b026f28cddac54448b2a4c1b7d
https://doi.org/10.2174/1570193x113106660020
https://doi.org/10.2174/1570193x113106660020
Autor:
Shantanu D. Shinde, Firoz A. Kalam Khan, Abhay S. Zambare, Jaiprakash N. Sangshetti, Sureshchandra P. Zambare
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cff42a8494cb7250f4b153222483a5f
https://doi.org/10.1002/chin.201619234
https://doi.org/10.1002/chin.201619234
Publikováno v:
Chinese Chemical Letters. 20:171-174
Oxalic acid has been used as a catalyst for intramolecular cyclisation of 2-hydroxychalcones to form flavones in good yields. The efficiency of the catalyst was proved with a variety of substrates ranging from electron-deficient to electron-rich aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8b605cc062c9a198e4086ac66b372e7
https://doi.org/10.1016/j.cclet.2008.10.042
https://doi.org/10.1016/j.cclet.2008.10.042
Publikováno v:
ChemInform. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bcab228df8086bb525856a403415908
https://doi.org/10.1002/chin.201503255
https://doi.org/10.1002/chin.201503255
Publikováno v:
ChemInform. 40
Oxalic acid has been used as a catalyst for intramolecular cyclisation of 2-hydroxychalcones to form flavones in good yields. The efficiency of the catalyst was proved with a variety of substrates ranging from electron-deficient to electron-rich aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce875a7de36ea1b349a6a7b3ddd18997
https://doi.org/10.1002/chin.200925129
https://doi.org/10.1002/chin.200925129