Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Trapti Aggarwal"'
Publikováno v:
The Journal of Organic Chemistry. 88:2474-2486
Publikováno v:
Advanced Synthesis & Catalysis. 363:4555-4560
Publikováno v:
Organic Chemistry Frontiers. 8:6452-6468
The fusion of fluorine in drug molecules through different fluorinating reagents remains a cornerstone in pharmaceutical chemistry. Progress in the field of deoxyfluorination through the development of novel reagents has enabled new mechanistic appro
Publikováno v:
European Journal of Organic Chemistry. 2020:3312-3316
Publikováno v:
Organic & Biomolecular Chemistry. 18:7056-7073
The diverse biological activities of nitrogen-containing compounds make the construction of the C-N bond of great importance. As N-fluorobenzenesulfonimide, one of the most abundant chemical feedstock, has a dual behaviour, i.e. as an electrophilic f
Publikováno v:
Chemistry – A European Journal. 25:16063-16067
Publikováno v:
Organicbiomolecular chemistry. 17(36)
Carbazoles are privileged nitrogen heterocycles that are present in a wide range of natural products, pharmaceuticals, and functional materials. Due to their wide application, various synthetic strategies are available in the literature using substit
Autor:
Akhilesh K. Verma, Trapti Aggarwal
Publikováno v:
Protecting-Group-Free Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1da965785b405ea946035c8f4033b675
https://doi.org/10.1002/9781119295266.ch5
https://doi.org/10.1002/9781119295266.ch5
Publikováno v:
Tetrahedron Letters. 55:2603-2608
A tandem approach for the regio- and stereoselective synthesis of oxazolo-fused pyrroloquinolines 3a – l via the reaction of o -alkynylaldehydes 1a – i with chiral amino alcohols 2a – c under mild reaction conditions is described. The possible
Autor:
Akhilesh K. Verma, Siva K. Reddy Kotla, Rakesh Tiwari, Sonu Kumar, Hemlata Nimesh, Trapti Aggarwal
Publikováno v:
The Journal of Organic Chemistry. 78:5372-5384
An efficient cascade strategy for the direct synthesis of pyrrolo[3,2,1-de]acridones 4a-v, 5a-h from iodo-pyranoquinolines 2a-i by the palladium-catalyzed regioselective [3 + 2] alkyne annulation/ring-opening followed by intramolecular aldol condensa