Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sivaparwathi, Golla"'
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
Publikováno v:
Organicbiomolecular chemistry. 20(24)
A sequential one-pot classical aldol, transition-metal and hydride-free reductive aldol reaction is reported here for C(sp3)- H functionalization of 2-oxindoles using the multifaceted reagent rongalite. Here, rongalite functions as a hydride-free red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ba2cc25556315bb60e30a34b70c256a
https://pubmed.ncbi.nlm.nih.gov/35506377
https://pubmed.ncbi.nlm.nih.gov/35506377
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:
Materials Today Communications. 31:103753
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9e954b2b6d7717a0e8f2643a6c9e6f3
https://doi.org/10.1016/j.mtcomm.2022.103753
https://doi.org/10.1016/j.mtcomm.2022.103753
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