Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Palaniappan Sakthivel"'
Publikováno v:
In Alexandria Engineering Journal January 2023 62:279-289
Autor:
Thangavelu, Kalavathi Devi, Murugesan, Madhan Mohan, Natarajan, Baluprithviraj Krishnasamy, Sreerangasamy, Uma Devi, Palaniappan, Sakthivel, Balasubramaniam, Sangavi, Kalpana, Shubhashree Venkatesh
Publikováno v:
AIP Conference Proceedings; 2023, Vol. 2857 Issue 1, p1-11, 11p
Publikováno v:
Indonesian Journal of Electrical Engineering & Computer Science; Dec2023, Vol. 32 Issue 3, p1278-1287, 10p
Akademický článek
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Autor:
Kalimuthusamy Natarajaseenivasan, Charles Solomon Akino Mercy, Andivelu Ilangovan, Palaniappan Sakthivel, Karikalacholan Sivasankari
Publikováno v:
European Journal of Medicinal Chemistry. 125:29-40
A simple and efficient method for the synthesis of a series of 6,7-dihydro-3H-pyrano[4,3-c]isoxazol-3-one derivatives starting from 5-carboalkoxy-2,3-dihydropyranone (5-CDHPs) has been developed. Pyranoisoxazolones 10a-j, dihydronaphthopyran-4-one (D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ba004bce45f904a9bca4f72c9f90760
https://doi.org/10.1016/j.ejmech.2016.09.020
https://doi.org/10.1016/j.ejmech.2016.09.020
Publikováno v:
ChemistrySelect. 1:1109-1116
A variety of 5-aroyl/alkanoyl-2,3-dihydro-4H-pyran-4-ones have been synthesised by reaction between acyclic beta-diketones and alpha, beta-unsaturated acyl chlorides in the presence of CaCl2 as catalyst. The reaction proceeds via domino C-acylation/6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cec337eb80d794daf5aa8c29935f733
https://doi.org/10.1002/slct.201600131
https://doi.org/10.1002/slct.201600131
Publikováno v:
Organic Chemistry Frontiers. 3:1680-1685
A simple one-pot procedure for conversion of 2-iodo/2-nitro benzoic acids and dihydropyranone fused benzoic acids into corresponding anilines, using tosyl azide, under transition metal-free conditions is explained. TsN3, is one of the more stable azi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad7e342c994d7fb6fb505e2eb6d9e930
https://doi.org/10.1039/c6qo00343e
https://doi.org/10.1039/c6qo00343e
Publikováno v:
RSC Adv.. 4:55150-55161
Intermolecular domino C-acylation/6π-oxaelectrocyclization between β-ketoesters and α,β-unsaturated acid chlorides took place readily in the presence of CaCl2 to afford a variety of polysubstituted 5-carboalkoxy-2,3-dihydro-4H-pyran-4-ones, in go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c676f520ae0af46b181a7ebde7a28bb3
https://doi.org/10.1039/c4ra11174e
https://doi.org/10.1039/c4ra11174e
Publikováno v:
Australian Journal of Electrical & Electronic Engineering; Dec2020, Vol. 17 Issue 4, p263-268, 6p
Publikováno v:
ChemInform. 47
A variety of 5-aroyl/alkanoyl-2,3-dihydro-4H-pyran-4-ones have been synthesised by reaction between acyclic beta-diketones and alpha, beta-unsaturated acyl chlorides in the presence of CaCl2 as catalyst. The reaction proceeds via domino C-acylation/6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc881fbf746ed72be60b0a2fa7fc10fc
https://doi.org/10.1002/chin.201637106
https://doi.org/10.1002/chin.201637106