Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Rajender Nallagonda"'
Publikováno v:
ACS Catalysis. 12:1818-1829
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0058eb10c1058a4a1139bf49b96b0541
https://doi.org/10.1021/acscatal.1c05780
https://doi.org/10.1021/acscatal.1c05780
Autor:
Rajender Nallagonda, Rashad R. Karimov
Publikováno v:
ACS Catalysis. 11:248-254
Nucleophilic addition of diborylalkyl reagents to N-alkyl or N-acylpyridinium and related heteroarenium salts has been developed as a key step for the synthesis of nonaromatic nitrogen heterocycles...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38d7d977a21ba400860c7c7125338cc7
https://doi.org/10.1021/acscatal.0c04474
https://doi.org/10.1021/acscatal.0c04474
Autor:
Rajasekhar Reddy Reddy, Israa Shioukhi, Nivesh Kumar, Ahmad Masarwa, Hila Sagi, Rajender Nallagonda
Publikováno v:
PATAI'S Chemistry of Functional Groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7c5864d6e3e1d9fe3dc83d638951b85
https://doi.org/10.1002/9780470682531.pat0975
https://doi.org/10.1002/9780470682531.pat0975
Publikováno v:
Organic & Biomolecular Chemistry. 16:1050-1064
Recently, gem-diborylalkanes have attracted much attention as versatile building blocks and fundamental intermediates in organic synthesis, because they enable multiple C-C bond construction and further transformation at C-B bonds. Importantly, gem-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda1ff46c6073fbbdfda09a5304c8e6f
https://doi.org/10.1039/c7ob02978k
https://doi.org/10.1039/c7ob02978k
Publikováno v:
Advanced Synthesis & Catalysis. 360:255-260
Cobalt-catalyzed sp(2) C-H bond functionalization of diarylphosphinamides with heterobicyclic alkenes was demonstrated at room temperature employing commercially available cobalt(II)-salts. The effectiveness of this strategy was illustrated with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1d6f2c9cbd88d83907adac662ae8921
https://doi.org/10.1002/adsc.201701162
https://doi.org/10.1002/adsc.201701162
Publikováno v:
Organicbiomolecular chemistry. 15(35)
A palladium-catalyzed oxidation reaction is disclosed where the nitrile functionality on the substrate simply changes the course of the reaction. Our previous finding showed that using the Pd(II)-catalyst in the presence of benzoquinone as an oxidant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede9de0f1ba79de2bfa7838186b5c7ec
https://pubmed.ncbi.nlm.nih.gov/28825438
https://pubmed.ncbi.nlm.nih.gov/28825438
Publikováno v:
The Journal of organic chemistry. 82(7)
Disclosed herein is an efficient synthetic route for the synthesis of functionalized 2-benzyl benzo[b]furans via a regioselective 5-exo-trig intramolecular oxidative cyclization of ortho-cinnamyl phenols using [PdCl2(CH3CN)2] as catalyst and benzoqui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e5f8eac9e0acc35b9d959537227616c
https://pubmed.ncbi.nlm.nih.gov/28249386
https://pubmed.ncbi.nlm.nih.gov/28249386
Publikováno v:
Organic Letters. 16:4786-4789
An efficient strategy for the synthesis of 3-substituted 2-benzylindoles from stable and readily available o-allylanilines, prepared from anilines and allyl alcohols, has been developed. The reaction occurred via a regioselective 5-exo-trig intramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7b1a06d3db73ce22cb835aa5f60709
https://doi.org/10.1021/ol502244g
https://doi.org/10.1021/ol502244g
Publikováno v:
ChemInform. 47
An efficient preparation of various highly substituted 2-benzyl furans is developed starting from 2-cinnamyl-1,3-dicarbonyl derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a2d9233a1ae5da5251633ed8f32fe8
https://doi.org/10.1002/chin.201611124
https://doi.org/10.1002/chin.201611124
Publikováno v:
ChemInform. 47
The new catalysts are applied to the asymmetric reduction of a wide range of ketimines, the syntheses of enantiopure α-amino esters, γ- and δ-lactams, isoindolinones, and pharmaceutically relevant targets, such as (R)-(+)-salsolidine and (R)-(+)-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::152b91f0aa9ae9179000e9eea55cafcf
https://doi.org/10.1002/chin.201602020
https://doi.org/10.1002/chin.201602020