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pro vyhledávání: '"Fazlur-Rahman Nawaz Khan"'
Publikováno v:
ACS Omega, Vol 9, Iss 34, Pp 36198-36219 (2024)
Externí odkaz:
https://doaj.org/article/0299014584be46e8862e60d060ad959c
Publikováno v:
The Scientific World Journal, Vol 2012 (2012)
The diversified bis-isoquinolinones were obtained in two steps, utilizing homophthalic acid and various acid chlorides providing 3-substituted isocoumarins in the first step which on further condensation with 1,7-heptadiamine involving C–N bond for
Externí odkaz:
https://doaj.org/article/ef7f309062c444d28baee70d048eb97b
Akademický článek
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Akademický článek
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Publikováno v:
ACS Omega; 6/11/2024, Vol. 9 Issue 23, p24464-24476, 13p
Publikováno v:
ACS Omega, Vol 4, Iss 5, Pp 8046-8055 (2019)
Externí odkaz:
https://doaj.org/article/dd43e96c53074e65841f7d8855d5fbcb
Autor:
Chitrala Teja, Hanumanthu Roshini, Pandurangan Thiyagamurthy, J. Arul Daniel, S. Asha Devi, R. Vidya, Fazlur Rahman Nawaz Khan
Publikováno v:
Polycyclic Aromatic Compounds. 43:699-720
A series of quinoline-chalcones were synthesized from one-pot Friedlander annulation followed by Claisen–Schmidt condensation in the presence of tetrabutylammonium-ionic liquids (TBA-ILs) as a catalyst and base medium under MW-Irradiation. TBA-ILs
Heterocyclic compounds play an important role in drug design and discovery, and they have been used to treat a variety of diseases, including cancer. Cancer is one of the leading causes of death in the world. However, various drugs and therapies are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17bc19adc7b507ec3e34e4d6aade8b6f
https://doi.org/10.2174/9789815040074122010008
https://doi.org/10.2174/9789815040074122010008
Publikováno v:
Polycyclic Aromatic Compounds. 42:4466-4474
An efficient synthesis of 1,1,3-trisubstituted-1H-isochromenes, 3 is reported from isochromen-1-ones, 1 and Grignard Reagents, 2a-h through sequential Grignard reactions/acid-catalyzed cyclization....
Publikováno v:
Chemistry – An Asian Journal. 15:4153-4167
Quinoline is considered one of the most ubiquitous heterocycles due to its engaging biological activities and synthetic utility over organic transformations. Over the past few decades, numerous reports have been documented in the synthesis of quinoli