Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Mani, Ramanathan"'
Autor:
Ziad Moussa, Mani Ramanathan, Shaikha Mohammad Alharmoozi, Shahad Ali Saeed Alkaabi, Salamah Hamdan Mohammed Al Aryani, Saleh A. Ahmed, Harbi Tomah Al-Masri
Publikováno v:
Heliyon, Vol 10, Iss 20, Pp e38894- (2024)
Aza-heterocyclic scaffolds are privileged cores in the composition of their potential therapeutic profiles and versatile synthetic intermediates. Pyrazole is one of the frequently studied compounds of “azole” family and consists of nitrogen in a
Externí odkaz:
https://doaj.org/article/17e7652cc95a4f3d93f6bcec372fa807
Autor:
Amin F. Majdalawieh, Anusha Sebastian, Mani Ramanathan, Vunnam Srinivasulu, Monther A. Khanfar, Scott McN. Sieburth, Imad A. Abu-Yousef, Taleb H. Al-Tel
Publikováno v:
The Journal of Organic Chemistry. 86:12872-12885
The indolo[2,3-a]quinolizines, canthines, and arborescidines natural products exhibit a wide range of bioactivities including anticancer, antiviral, antibacterial, and anti-inflammatory, among others. Therefore, the development of modular and efficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63ac33d86177446300026a114a35a0de
https://doi.org/10.1021/acs.joc.1c01523
https://doi.org/10.1021/acs.joc.1c01523
Autor:
Taleb H. Al-Tel, Vunnam Srinivasulu, Farah Al-Marzooq, Mohamad Hamad, Monther A. Khanfar, Mani Ramanathan, Nelson C. Soares
Publikováno v:
Synthesis. 53:1911-1922
We present a divergent strategy that permits access to diversely functionalized benzoxazepinium scaffolds fused to various heterocycles. The described strategy features a one-pot combination of the Groebke–Blackburn–Bienaymé reaction and an aza-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9abf3b2786ed5036ce303dd8043521f7
https://doi.org/10.1055/s-0040-1706006
https://doi.org/10.1055/s-0040-1706006
Autor:
Mani Ramanathan, Duen-Ren Hou
Publikováno v:
ARKIVOC, Vol 2013, Iss 3, Pp 98-108 (2013)
Externí odkaz:
https://doaj.org/article/84c96fb5e93e44a9a6018c5dce0c3b85
Autor:
Anusha Sebastian, Amin F. Majdalawieh, Vunnam Srinivasulu, Mani Ramanathan, Maria Laura Bolognesi, Imad A. Abu-Yousef, Taleb H. Al-Tel, Nelson C. Soares
Publikováno v:
Organic & Biomolecular Chemistry. 18:8526-8571
The last two decades or so have witnessed an upsurge in defining the art of designing complex natural products and nature-inspired molecules. Throughout these decades, fundamental insights into stereocontrolled, step-economic and atom-economical synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f9b35e7c1a24016b4d456ed1a9c8238
https://doi.org/10.1039/d0ob01550d
https://doi.org/10.1039/d0ob01550d
Autor:
Vunnam, Srinivasulu, Scott McN, Sieburth, Monther A, Khanfar, Imad A, Abu-Yousef, Amin, Majdalawieh, Mani, Ramanathan, Anusha, Sebastian, Taleb H, Al-Tel
Publikováno v:
The Journal of organic chemistry. 86(18)
The indolo[2,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce1203c16ec95fd63386e0aee8ba8bc9
https://pubmed.ncbi.nlm.nih.gov/34477383
https://pubmed.ncbi.nlm.nih.gov/34477383
Publikováno v:
The Journal of Organic Chemistry. 84:7459-7467
An easy manipulation method for the preparation of N-arylquinazolinium salts is described from readily available aryldiazonium salts, nitriles, and 2-aminoarylketones in a one-pot operation. This method relies on the in situ generation of the N-aryln
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eadfad3309766709cde911622e28ba52
https://doi.org/10.1021/acs.joc.9b00601
https://doi.org/10.1021/acs.joc.9b00601
Publikováno v:
Tetrahedron. 75:791-796
One-pot synthesis of 3-aryl-4(3H)-quinazolinones has been realized through a cascade annulation. Reaction of aryldiazonium salt with a nitrile provides in situ generation of a reactive nitrilium ion, which is attacked by the amino group of 2-aminoben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50d2b0b231531e7ce5523611295bd548
https://doi.org/10.1016/j.tet.2018.12.065
https://doi.org/10.1016/j.tet.2018.12.065
Publikováno v:
Organicbiomolecular chemistry. 18(5)
A new method for the preparation of 2-amino-3-cyanoquinolines from readily available aryldiazonium salts, 2-aminoarylketones, and malononitrile via a cascade reaction is reported. This one-pot approach involves the in situ generation of an N-arylnitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fdd2a45da6b0b5b08d7b20fc5ae51de
https://pubmed.ncbi.nlm.nih.gov/31932827
https://pubmed.ncbi.nlm.nih.gov/31932827
Publikováno v:
The Journal of Organic Chemistry. 83:6133-6141
A transition-metal-free approach for the preparation of N-arylketimines has been developed from the direct reaction of aryldiazonium salts, arenes, and nitriles in a one-pot fashion with the consecutive formation of N-C and C-C bonds. This approach p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7efa5a447887658bbbf2c4b7bf089ed6
https://doi.org/10.1021/acs.joc.8b01000
https://doi.org/10.1021/acs.joc.8b01000