Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Muppidi Subbarao"'
Autor:
Anthony Saucedo, Muppidi Subbarao, Mauricio Jemal, Nakya L. Mesa-Diaz, Jadyn L. Smith, Alexandra Vernaza, Liqin Du, Sean M. Kerwin
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8051 (2024)
Caffeic acid phenethyl ester (CAPE) is a phenolic natural product with a wide range of biological activities, including anticancer activity; however, the ester group of CAPE is metabolically labile. The corresponding amide, CAPA, has improved metabol
Externí odkaz:
https://doaj.org/article/b6e44c4e93ec4885961c970c33f16bbf
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:
Advanced Synthesis & Catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::217c5802d47e0a74e8e366309a8e848c
https://doi.org/10.1002/adsc.202300204
https://doi.org/10.1002/adsc.202300204
Publikováno v:
Organic & Biomolecular Chemistry. 19:8241-8245
Highly regio- and stereoselective palladium-catalyzed ortho-vinylation of β-naphthols (2) has been reported using easily accessible CF3-allyl carbonates (1). The regioselective nucleophilic γ-attack of the CF3–π-allyl–Pd-intermediate is the ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b443f2d97de71cc48483d8c2501480e6
https://doi.org/10.1039/d1ob01429c
https://doi.org/10.1039/d1ob01429c
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
Publikováno v:
Organicbiomolecular chemistry. 19(38)
Highly regio- and stereoselective palladium-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c0338132581556f4b5ef7926da12be9
https://pubmed.ncbi.nlm.nih.gov/34505862
https://pubmed.ncbi.nlm.nih.gov/34505862
Publikováno v:
Organic Letters
Organic Letters, 2021, 23 (12), pp.4882-4887. ⟨10.1021/acs.orglett.1c01615⟩
Organic Letters, 2021, 23 (12), pp.4882-4887. ⟨10.1021/acs.orglett.1c01615⟩
International audience; A domino propargylation/furanylation (intramolecular exo-dig-cyclization)/benzannulation reaction of 2,4-diyn-1-ols with 1,3-dicarbonyl compounds has been developed for the first time. This provides a novel and effective metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88fae977c07fdc01233c041111173710
https://hal.archives-ouvertes.fr/hal-03282736
https://hal.archives-ouvertes.fr/hal-03282736
Publikováno v:
Chemical Data Collections. 39:100865
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2e76b9395356152708d55e0788eb310
https://doi.org/10.1016/j.cdc.2022.100865
https://doi.org/10.1016/j.cdc.2022.100865
Autor:
Chada Raji Reddy, Muppidi Subbarao, Ramachandra Reddy Donthiri, Puppala Sathish, Ejjirotu Srinivasu
Publikováno v:
The Journal of organic chemistry. 86(1)
Arylative annulation of 2-carbonyl-3-propargyl indoles with boronic acids under sequential palladium/triflic acid catalysis is described. The present strategy to provide di- and triaryl carbazoles in one pot involves benzannulation through difunction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e0c14cd9fbca6bc1c3c4ae874bcbe4
https://pubmed.ncbi.nlm.nih.gov/33322899
https://pubmed.ncbi.nlm.nih.gov/33322899
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