Zobrazeno 1 - 10
of 865
pro vyhledávání: '"E. Muraglia"'
Autor:
Kumar, Dharmendra1 dharmendrabrooke@gmail.com, Bhargava, Mahesh Kumar2, Shahi, Apra2, Singh, Randhir2, Tandia, Neelam1, Singh, Priya1
Publikováno v:
Indian Journal of Veterinary Sciences & Biotechnology. Sep/Oct2024, Vol. 20 Issue 5, p21-25. 5p.
Autor:
Enrico Baciocchi, E. Muraglia
Publikováno v:
Tetrahedron Letters. 35:2763-2766
An efficient synthesis of γ-haloesters has been achieved, under very mild conditions, by addition of electrophilic carbon radicals ·CH(R)CO2Et (R=H, Me, CO2Et) generated by XCH(R)CO2Et (X=Br, I) / BEt3 / air in DMSO to alkenes and cycloalkenes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3bf24453b2615b95dd2bdec19e37312
https://doi.org/10.1016/s0040-4039(00)77027-4
https://doi.org/10.1016/s0040-4039(00)77027-4
Autor:
E. Muraglia, Enrico Baciocchi
Publikováno v:
Tetrahedron Letters. 34:5015-5018
An efficient homolytic aromatic substitution of pyroles, furan and thiophene by ·CH2CO2Et and ·CH(CH3)CO2Et has been carried out, the radicals being generated by autoxidation of BEt3 in the presence of XCH2CO2Et and XCH(CH3)CO2Et (X=Br, I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9ac69b79760793d87d8e9ec6803bfbd
https://doi.org/10.1016/s0040-4039(00)74072-x
https://doi.org/10.1016/s0040-4039(00)74072-x
Publikováno v:
The Journal of Organic Chemistry. 58:2013-2016
Homolytic substitutions of ferrocene with a variety of carbon-centered radicals have been investigated. Reactions with synthetic utility have only been obtained in the cases of ambiphilic radicals (cyanomethyl and alkoxycarbonylmethyl), whereas nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f7233338f474ce9e29ffb5adb83817c
https://doi.org/10.1021/jo00060a011
https://doi.org/10.1021/jo00060a011
Publikováno v:
ChemInform. 23
The intramolecular selectivity in the side-chain oxidation of alkylbenzenes, under the GifIV conditions, has been determined. The 1°-C: 2°-C: 3°-C reactivity ratios are 1:5: 9.3 and little difference in reactivity is exhibited by methyl groups par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9d6a829c6c2d324783ea47575224304
https://doi.org/10.1002/chin.199212090
https://doi.org/10.1002/chin.199212090
Publikováno v:
ChemInform. 24
Efficient and selective homolytic substitutions (yield between 55 and 90%) of pyrrole, indole, and some pyrrole derivatives have been carried out using ambiphilic and electrophilic carbon centered radicals, generated in DMSO by Fe 2+ /H 2 O 2 and α-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23317c176119100aa36844953ce9d00c
https://doi.org/10.1002/chin.199318072
https://doi.org/10.1002/chin.199318072
Publikováno v:
ChemInform. 24
Homolytic substitutions of ferrocene with a variety of carbon-centered radicals have been investigated. Reactions with synthetic utility have only been obtained in the cases of ambiphilic radicals (cyanomethyl and alkoxycarbonylmethyl), whereas nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a8d975af6a37c14a1022ef8c5c783ca
https://doi.org/10.1002/chin.199333237
https://doi.org/10.1002/chin.199333237
Autor:
Enrico Baciocchi, E. Muraglia
Publikováno v:
ChemInform. 24
An efficient synthesis of perfluoroalkylpyrroles has been performed by reaction of pyrroles and some derivatives with perfluoroalkyl radicals generated by perfluoroalkyl iodides/ H2O2/ Fe+2 in DMSO at room temperature.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::661aab89629a0d6923ce1fd8371526d8
https://doi.org/10.1002/chin.199344162
https://doi.org/10.1002/chin.199344162
Autor:
E. Muraglia, Enrico Baciocchi
Publikováno v:
ChemInform. 24
An efficient homolytic aromatic substitution of pyroles, furan and thiophene by ·CH2CO2Et and ·CH(CH3)CO2Et has been carried out, the radicals being generated by autoxidation of BEt3 in the presence of XCH2CO2Et and XCH(CH3)CO2Et (X=Br, I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83d4d28706d7cfa004eb218bcd3ba570
https://doi.org/10.1002/chin.199343123
https://doi.org/10.1002/chin.199343123
Autor:
Enrico Baciocchi, E. Muraglia
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09190f50bcc27660cfc2551350ccbf95
https://doi.org/10.1002/chin.199417084
https://doi.org/10.1002/chin.199417084