Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Dattahari H. Kolgave"'
Autor:
Chada Raji Reddy, Muppidi Subbarao, Dattahari H. Kolgave, Uprety Ajaykumar, Puthiya Purayil Vinaya
Publikováno v:
ACS Omega. 7:38045-38052
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac0e18f12bf8335dc10bc995b8d4560c
https://doi.org/10.1021/acsomega.2c05394
https://doi.org/10.1021/acsomega.2c05394
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6e6c04c177b6a5b260c2ff04d57896a
https://doi.org/10.1021/acs.joc.3c00374
https://doi.org/10.1021/acs.joc.3c00374
Publikováno v:
Organic & Biomolecular Chemistry. 20:6879-6889
A diverse range of diketoalkylated spiro-trienones involving a copper(ii)-catalyzed cascade radical addition/ipso-annulation/dearomatization reaction of N-arylpropiolamides and biaryl ynones are synthesized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48918635fdd6f119a72ac5c172ff0541
https://doi.org/10.1039/d2ob01282k
https://doi.org/10.1039/d2ob01282k
Autor:
Dattahari H. Kolgave, Chada Raji Reddy
Publikováno v:
The Journal of Organic Chemistry. 86:17071-17081
Electrooxidative-induced synthesis of structurally diverse seleno-dibenzocyclohepten-5-ones and seleno-spiro[5.5]trienones by selenylative carbannulation of biaryl ynones with diaryl diselenide has been developed. The switchable reactivity, intramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17b952f251424833b3a1fc5e7b0f131
https://doi.org/10.1021/acs.joc.1c02182
https://doi.org/10.1021/acs.joc.1c02182
Publikováno v:
Organicbiomolecular chemistry. 20(34)
An unprecedented copper-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a66b9cee069c4a72a5833e23a20481f9
https://pubmed.ncbi.nlm.nih.gov/35972321
https://pubmed.ncbi.nlm.nih.gov/35972321
Publikováno v:
The Journal of Organic Chemistry. 85:15521-15531
A facile oxidative dearomatization of N-(p-methoxyaryl)propiolamides has been established for the synthesis of spiro-fused 2,5-cyclohexadienone frameworks via thio(seleno)cyanative ipso-cyclization...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9481d6b6c6c916a032c0d5ab3760ab26
https://doi.org/10.1021/acs.joc.0c02270
https://doi.org/10.1021/acs.joc.0c02270
Autor:
Dattahari H. Kolgave, Chada Raji Reddy, Santosh Kumar Prajapti, Mounika Aila, Muppidi Subbarao
Publikováno v:
Organic Letters. 22:5342-5346
A strategy to functionalized spiro[4.5]trienones, by domino silver-catalyzed decarboxylative acylation or alkylation/ ipso-cyclization of N-arylpropiolamides with α-keto acids/alkyl carboxylic acids, is presented. This transformation offers a wide r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06b4e6c2d5e2e72113c376699dae281c
https://doi.org/10.1021/acs.orglett.0c01588
https://doi.org/10.1021/acs.orglett.0c01588
Autor:
Chada Raji, Reddy, Dattahari H, Kolgave, Muppidi, Subbarao, Mounika, Aila, Santosh Kumar, Prajapti
Publikováno v:
Organic letters. 22(14)
A strategy to functionalized spiro[4.5]trienones, by domino silver-catalyzed decarboxylative acylation or alkylation/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::04ab6cf9d32e89c343724d7a9c0876a6
https://pubmed.ncbi.nlm.nih.gov/32603125
https://pubmed.ncbi.nlm.nih.gov/32603125
Autor:
Dattahari H. Kolgave, Muppidi Subbarao, Puppala Sathish, Ramachandra Reddy Donthiri, Chada Raji Reddy
Publikováno v:
Organic letters. 22(2)
A novel strategy for the synthesis of 3-hydroxycarbazoles involving the consecutive propargylation/palladium-catalyzed hydroxylative benzannulation of indole-2-carbonyls with propargylic alcohols has been exploited. This one-pot procedure leads to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ac9973f3903284cc174b06177914297
https://pubmed.ncbi.nlm.nih.gov/31909623
https://pubmed.ncbi.nlm.nih.gov/31909623
Publikováno v:
Organic & Biomolecular Chemistry; 6/28/2024, Vol. 22 Issue 24, p4771-4777, 7p