Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hari Prasad Kokatla"'
Publikováno v:
The Journal of Organic Chemistry. 87:10435-10440
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64ade4f3a743f27865e0256f8ebffc03
https://doi.org/10.1021/acs.joc.2c00904
https://doi.org/10.1021/acs.joc.2c00904
Publikováno v:
Organic & Biomolecular Chemistry. 20:808-816
A transition-metal and hydride-free reductive aldol reaction has been developed for the synthesis of biologically active 3,3'-disubstituted oxindoles from isatin derivatives using rongalite. In this protocol, rongalite plays a dual role as a hydride-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5a287fb8dc696447c7f2d7b1ee84d42
https://doi.org/10.1039/d1ob02284a
https://doi.org/10.1039/d1ob02284a
Publikováno v:
Organic & Biomolecular Chemistry. 20:4926-4932
Rongalite induced transition metal and hydride-free reductive aldol reaction is developed for 3-methylindoline-2-ones and 3-(hydroxymethyl)-3-methylindolin-2-ones from 2-oxindoles. Here, Rongalite plays a key role of being a reductant and C1 source.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0142a4a162626f14c7525386575713f
https://doi.org/10.1039/d2ob00665k
https://doi.org/10.1039/d2ob00665k
Publikováno v:
Advanced Synthesis & Catalysis. 364:149-157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a29cc92a92c519c65a14acb308d8144
https://doi.org/10.1002/adsc.202100883
https://doi.org/10.1002/adsc.202100883
Publikováno v:
The Journal of organic chemistry. 87(15)
A transition metal- and hydride-free protocol has been developed for the chemoselective reduction of α-keto esters and α-keto amides using rongalite as a reducing agent. Here, rongalite acts as a hydride-free reducing agent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84162ea908ee8563670b205e64b56638
https://pubmed.ncbi.nlm.nih.gov/35839148
https://pubmed.ncbi.nlm.nih.gov/35839148
Autor:
Sivaparwathi Golla, Sanjeeva Thunga, Hari Prasad Kokatla, Soumya Poshala, Vanaparthi Satheesh
Publikováno v:
ChemistrySelect. 4:10466-10470
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68b23d0a4cb70c63883f1a91b71222c6
https://doi.org/10.1002/slct.201902189
https://doi.org/10.1002/slct.201902189
Publikováno v:
ChemistrySelect. 3:13759-13764
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c63eef67e6bf04f886c9b60aac0e7e9b
https://doi.org/10.1002/slct.201802584
https://doi.org/10.1002/slct.201802584
Publikováno v:
ChemistrySelect. 3:4425-4429
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52db59b15e29f50ea4826e2da856f29a
https://doi.org/10.1002/slct.201800564
https://doi.org/10.1002/slct.201800564
Autor:
Hari Prasad Kokatla, Soumya Poshala, Ramaiah Konakanchi, Naveenkumar Anugu, Satheesh Vanaparthi, Sanjeeva Thunga
Publikováno v:
Tetrahedron Letters. 60:2046-2048
An efficient new Pd(II)-(2-aminonicotinaldehyde)-catalyzed Suzuki-Miyaura coupling of the aryl halides (Br, Cl and I) and organoboronic acids at moderate temperature in water is described. Low catalyst loading, easy accessibility, being an air-stable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c782590073aa67a159ea493cefefa9ff
https://doi.org/10.1016/j.tetlet.2019.06.051
https://doi.org/10.1016/j.tetlet.2019.06.051
Publikováno v:
Tetrahedron Letters. 61:151539
A novel rongalite-promoted metal-free aerobic ipso-hydroxylation of arylboronic acids has been developed. This method employs low-cost rongalite as a radical initiator and O2 as a green oxidizing agent for ipso-hydroxylation. This protocol is compati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aa61e1fe57a99d8db0a99e99eb2aaf9
https://doi.org/10.1016/j.tetlet.2019.151539
https://doi.org/10.1016/j.tetlet.2019.151539