Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Alagiri Kaliyamoorthy"'
Publikováno v:
The Journal of Organic Chemistry. 88:2655-2665
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2eb75ec28c3a55e84f56010ca690617
https://doi.org/10.1021/acs.joc.2c03001
https://doi.org/10.1021/acs.joc.2c03001
Autor:
Varun, Begur Vasanthkumar, Dhineshkumar, Jayaraman, Bettadapur, Kiran R., Siddaraju, Yogesh, Alagiri, Kaliyamoorthy, Prabhu, Kandikere Ramaiah
Publikováno v:
In Tetrahedron Letters 1 March 2017 58(9):803-824
Publikováno v:
The Journal of Organic Chemistry. 87:14980-14990
Heteroaryl sulfoxides are an integral part of several bioactive molecules and pharmaceuticals. We have described a transition-metal-free route for the direct sulfinylation of 2-halobenzothiazoles and 2-halobenzimidazoles using β-sulfinyl esters as t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a74cb5d7f0bec4eedc4107472818112
https://doi.org/10.1021/acs.joc.2c02153
https://doi.org/10.1021/acs.joc.2c02153
Autor:
Amritha Rayaroth, Afna Elikkottil, Chithra Mohan Jayakumari, Kalyanakrishnan Arayil Vennoli, Sivaranjana Reddy Vennapusa, Alagiri Kaliyamoorthy
Publikováno v:
Chemical Communications. 58:10671-10674
We have developed Brønsted base-mediated regioselective allenylation and propargylation of various para-quinone methides using unfunctionalized 2-alkynyl azaarenes as pronucleophiles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5d2a0a0e43f4c84d57f1a1ef2a8d216
https://doi.org/10.1039/d2cc03439e
https://doi.org/10.1039/d2cc03439e
Publikováno v:
ChemistrySelect. 6:14054-14059
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d245e52f54b32e59cc57203374c24cff
https://doi.org/10.1002/slct.202103939
https://doi.org/10.1002/slct.202103939
Autor:
Krishna Hari, Alagiri Kaliyamoorthy, Amritha Rayaroth, Rajat Kumar Singh, A V Kalyanakrishnan
Publikováno v:
Organic & Biomolecular Chemistry. 18:3354-3359
1,1,2-Triarylethanes embedded with an azaarene unit were prepared in a single step at ambient temperature via the sodium hexamethyldisilazide mediated 1,6-conjugate addition of unactivated alkylazaarenes on para-quinone methides (p-QMs). The extent o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97e211e8921133dbf0ac16d454711476
https://doi.org/10.1039/d0ob00419g
https://doi.org/10.1039/d0ob00419g
Publikováno v:
In Tetrahedron 2011 67(44):8544-8551
A straightforward synthesis of acylating reagents such as Weinreb and MAP amides from aromatic, aliphatic carboxylic acids, and amino acids using PPh3/NBS combination is described. A chemo-selective modification of the carboxylic acid group into Wein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98c0bb9680438856ce7d68e3606d7820
Publikováno v:
Tetrahedron Letters. 60:151131
A non-covalent Bronsted-basic N-heterocyclic carbene catalyzed (NHC) Friedel-Crafts type amination of naphthol derivatives using dialkyl azodicarboxylates as the aminating source and alcoholysis of various glutaric anhydrides using alcohol as pronucl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b81b792eaaa5325f69b9a187a6481e3
https://doi.org/10.1016/j.tetlet.2019.151131
https://doi.org/10.1016/j.tetlet.2019.151131
Publikováno v:
In Tetrahedron Letters 21 March 2012 53(12):1456-1459