Zobrazeno 1 - 10
of 10
pro vyhledávání: '"N. S. V. M. Rao Mangina"'
Publikováno v:
Organic & Biomolecular Chemistry. 17:2809-2817
An efficient method was developed for the synthesis of substituted aryl-fused pyrazolooxazepines from ortho-O-propargyl aryl pyrazoles by gold catalysis. In this organic transformation a new C-N bond was formed regioselectively via 7-exo-dig cyclizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bbe839cfa21e84af00a11e1c45b1958
https://doi.org/10.1039/c8ob03157f
https://doi.org/10.1039/c8ob03157f
Autor:
Galla V. Karunakar, Mukesh Sharma, Biraj Das, Kusum K. Bania, N. S. V. M. Rao Mangina, Anil Hazarika
Publikováno v:
Microporous and Mesoporous Materials. 272:31-39
Hierarchical structure in microporous zeolite-Y was introduced to overcome the diffusional restriction for direct encapsulation of chiral cobalt (II) Schiff base complexes. Mesopores with cylindrical channels of ∼5 nm dimensions were formed on post
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce8fa0c70b8cd8e6562e7c0b3a10d091
https://doi.org/10.1016/j.micromeso.2018.06.011
https://doi.org/10.1016/j.micromeso.2018.06.011
Autor:
Galla V. Karunakar, Kommuru Goutham, B. Sridhar, Veerabhushanam Kadiyala, Ravinder Guduru, N. S. V. M. Rao Mangina
Publikováno v:
Organic Letters. 19:282-285
An efficient gold-catalyzed synthesis of substituted 3-methylene-3,4-dihydrobenzo[b]oxepinones from ortho-O-propargyl substituted aryl enaminones has been achieved. In this transformation a new C-C bond formation occurred regioselectively via 7-exo-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9a994e0af5aa5d2fc0a655341b736e7
https://doi.org/10.1021/acs.orglett.6b03433
https://doi.org/10.1021/acs.orglett.6b03433
Publikováno v:
Organicbiomolecular chemistry. 16(12)
The reaction of arynes and secondary allylamines furnished ortho-allyl-substituted N-arylanilines via an aza-Claisen rearrangement. In this transformation, the sequential formation of C–C and C–N bonds occurred by involving two aryne molecules un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0306e982ea91d69c79bbf10e9086b4ac
https://pubmed.ncbi.nlm.nih.gov/29513309
https://pubmed.ncbi.nlm.nih.gov/29513309
Gold-catalysed cyclisation of N-propargylic β-enaminones to form 3-methylene-1-pyrroline derivatives
Autor:
Kommuru Goutham, N. S. V. M. Rao Mangina, Galla V. Karunakar, Pallepogu Raghavaiah, Surisetti Suresh
Publikováno v:
Org. Biomol. Chem.. 12:2869-2873
A gold(I) catalysed reaction between N-propargylic β-enaminones and arynes was developed to access 3-methylene-1-pyrrolines. The title compounds were obtained in 57-78% yields. This reaction is useful for the generation of substituted 1-pyrrolines e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d26fb40e1a3d12b7ecc7adc0940893f
https://doi.org/10.1039/c3ob42513d
https://doi.org/10.1039/c3ob42513d
Publikováno v:
ChemInform. 47
The reaction is proposed to proceed via aldehyde-assisted, gold-catalyzed oxidation/auration of the alkyne moiety, protodeauration of the organo-gold intermediate and cyclocondensation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ebcbff8e385f672e9cc9b62a84268b3
https://doi.org/10.1002/chin.201632184
https://doi.org/10.1002/chin.201632184
Publikováno v:
Organicbiomolecular chemistry. 14(14)
An efficient gold-catalyzed intramolecular cyclization of ortho-O-propargyl-1-one substituted arylaldehydes has been achieved for the generation of substituted aroylbenzo[b]oxepin-3-one derivatives in moderate to good yields. This synthetic transform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abda87eb8900aa123f60c2618cc5f21c
https://pubmed.ncbi.nlm.nih.gov/26974816
https://pubmed.ncbi.nlm.nih.gov/26974816
Autor:
N. S. V. M. Rao Mangina, Surisetti Suresh, Dalovai Purnachander, Galla V. Karunakar, Balasubramanian Sridhar, Vemu Nagaraju
Publikováno v:
ChemInform. 46
Synthesis of substituted 1,2-dihydropyridinones is described in a one pot reaction of β-enaminones and acetylene dicarboxylates where new C–C and C–N bonds were formed. The title compounds were obtained in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6809b1bb95eb2a0d4ba10384ef720b2
https://doi.org/10.1002/chin.201528195
https://doi.org/10.1002/chin.201528195
Autor:
Galla V. Karunakar, Surisetti Suresh, N. S. V. M. Rao Mangina, Dalovai Purnachander, Vemu Nagaraju, Balasubramanian Sridhar
Publikováno v:
Organicbiomolecular chemistry. 13(10)
Synthesis of substituted 1,2-dihydropyridinones is described in a one pot reaction of β-enaminones and acetylene dicarboxylates where new C–C and C–N bonds were formed. The title compounds were obtained in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::339ddb78641c1ecb14856fe00bcd5b02
https://pubmed.ncbi.nlm.nih.gov/25622067
https://pubmed.ncbi.nlm.nih.gov/25622067
Autor:
Pallepogu Raghavaiah, N. S. V. M. Rao Mangina, Kommuru Goutham, Galla V. Karunakar, Surisetti Suresh
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08fa8c240c653c2a60136188b845dfe9
https://doi.org/10.1002/chin.201444103
https://doi.org/10.1002/chin.201444103