Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Akash P. Sakla"'
Publikováno v:
Green Chemistry. 24:1259-1269
Microwave-assisted dithiocarbamation of various imidazoheterocycles with in situ generated dithiocarbamates via a water-soluble Cu(i) catalyst using benign solvent, enabling catalyst recyclability, scalability, less reaction time and high yields.
Autor:
Akash P. Sakla, Biswajit Panda, Ashutosh Mahale, Pravesh Sharma, Kritika Laxmikeshav, Mursalim Ali Khan, Onkar Prakash Kulkarni, Chandraiah Godugu, Nagula Shankaraiah
Publikováno v:
Bioorganic & Medicinal Chemistry. :117297
Publikováno v:
Organic & Biomolecular Chemistry. 19:7768-7791
Cycloaddition reactions are of great interest due to their potential and rapid construction of optically enriched spiro-cyclic products. 3-Methyleneindolinones have been proven to be a valuable precursor in cycloaddition reactions for the constructio
Autor:
Shankaraiah Nagula, Jay Prakash Soni, Akash P. Sakla, Biswajit Panda, Kritika Laxmikeshav, Sonal Bhandari, Chandraiah Godugu
Publikováno v:
Organic & Biomolecular Chemistry. 19:10622-10634
Herein, we report the first dithiocarbamation of spiro-aziridine oxindoles involving regiospecific ring-opening by in situ generated nucleophilic dithiocarbamates as an instant source of sulfur. This approach afforded C3-functionalised-3-thiooxindole
Publikováno v:
European Journal of Organic Chemistry. 2021:757-772
Publikováno v:
ChemistrySelect. 5:7004-7012
Autor:
Ahmed Kamal, Chander Singh Digwal, Chandraiah Godugu, Venu Talla, Nagula Shankaraiah, Amit Khurana, Sai Teja Nyalam, Akash P. Sakla, Upasana Yadav, Ramya Tokala
Publikováno v:
ChemistrySelect. 5:4356-4363
Publikováno v:
The Chemical Record. 20:253-272
The unprecedented efficiency, reliability and adaptability in drug discovery, with the growing number of applications and impact, have made Click Chemistry fascinating to the scientific community. The specificity, biocompatibility along with other pr
Publikováno v:
ChemistrySelect. 5:2886-2891
Publikováno v:
Organic & Biomolecular Chemistry. 18:8572-8596
Spiro-epoxy/aziridine oxindole frameworks are considered as an efficient structural toolbox to obtain C3-functionalised oxindole derivatives. These 3,3'-spiro-cyclic precursors are highly susceptible towards nucleophiles owing to their inherent ring