An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with α, α'-di- and trichloroketones
- Autor
- FEROCI, Marta1 ; INESI, Achille2 ; ORSINI, Monica2 ; ROSSI, Leucio2 ; SOTGIU, Giovanni3
[1] Dipartimento di Ing. Chim., Mater., Mat. Prim. e Metall., Università La Sapienza', Via del castro Laurenziano 7, 00161 Rome, Italy
[2] Dipartimento di Chimica, Ingegneria Chimica e Materiali, Università degli Studi, Monteluco di Roio, 67040 L'Aquila, Italy
[3] Dipartimento di Ingegneria Elettronica, Università di Roma Tre, Via Vasca Navale 84, 00146 Rome, Italy - Titulo de la publicación
- New trends in organic electrochemistry
- Autor ( monografía)
- NONAKA, T (Editor); SCHÄFER, H. J (Editor)1
[1] Organisch-Chemisches Institut der Universität Münster, Corrensstrasse 40, 48149 Münster, Germany - Fuente
Journal of electroanalytical chemistry (1992). 2001, Vol 507, Num 1-2, pp 89-95 ; ref : 19 ref
- ISSN
- 1572-6657
- Campo Científico
- General chemistry, physical chemistry; Metallurgy, welding
- Editor
- Elsevier Science, Amsterdam
- País de la publicación
- Netherlands
- Tipo de documento
- Article
- Idioma
- English
- Palabra clave (fr)
- Acylation Auxiliaire chiral Chimiosélectivité Composé chiral Etude expérimentale Halogénocétone Réaction électrochimique Réduction chimique Transposition Favorsky Oxazolidin-2-one(3-[3-méthylbut-2-énoyl]-4-phényl) Oxazolidin-2-one(4-phényl) Chlore Composé organique
- Palabra clave (in)
- Acylation Chiral auxiliary Chemoselectivity Chiral compound Experimental study Haloketone Electrochemical reaction Chemical reduction Favorsky rearrangement Chlorine Organic compounds
- Palabra clave (es)
- Acilación Auxiliar quiral Quimioselectividad Compuesto quiral Estudio experimental Halocetona Reacción electroquímica Reducción química Transposición Favorsky Cloro Compuesto orgánico
- Clasificación
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01H Electrochemistry / 001C01H05 Kinetics and mechanism of reactions
- Disciplina
- General chemistry and physical chemistry
- Procedencia
- Inist-CNRS
- Base de datos
- PASCAL
- Identificador INIST
- 1144931
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Acceso al documento
Install on your browser
DOI
10.1016/S0022-0728(01)00411-9 
https://dx.doi.org/10.1016/S0022-0728(01)00411-9
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:29:\"10.1016\/S0022-0728(01)00411-9\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:9:\"\u0000*\u0000jtitle\";s:45:\"Journal of electroanalytical chemistry (1992)\";s:9:\"\u0000*\u0000stitle\";s:28:\"J. electroanal. chem. (1992)\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:3:\"507\";s:8:\"\u0000*\u0000issue\";s:3:\"1-2\";s:8:\"\u0000*\u0000spage\";s:2:\"89\";s:8:\"\u0000*\u0000epage\";s:2:\"95\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1572-6657\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"FEROCI\";s:10:\"\u0000*\u0000aufirst\";s:5:\"Marta\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"INESI, Achille\";i:1;s:14:\"ORSINI, Monica\";i:2;s:13:\"ROSSI, Leucio\";i:3;s:16:\"SOTGIU, Giovanni\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:38:\"New trends in organic electrochemistry\";s:8:\"\u0000*\u0000title\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:8:\"\u0000*\u0000place\";s:9:\"Amsterdam\";s:6:\"\u0000*\u0000pub\";s:16:\"Elsevier Science\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Acceso mediante Panist
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:29:\"10.1016\/S0022-0728(01)00411-9\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:9:\"\u0000*\u0000jtitle\";s:45:\"Journal of electroanalytical chemistry (1992)\";s:9:\"\u0000*\u0000stitle\";s:28:\"J. electroanal. chem. (1992)\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:3:\"507\";s:8:\"\u0000*\u0000issue\";s:3:\"1-2\";s:8:\"\u0000*\u0000spage\";s:2:\"89\";s:8:\"\u0000*\u0000epage\";s:2:\"95\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1572-6657\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"FEROCI\";s:10:\"\u0000*\u0000aufirst\";s:5:\"Marta\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"INESI, Achille\";i:1;s:14:\"ORSINI, Monica\";i:2;s:13:\"ROSSI, Leucio\";i:3;s:16:\"SOTGIU, Giovanni\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:38:\"New trends in organic electrochemistry\";s:8:\"\u0000*\u0000title\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:8:\"\u0000*\u0000place\";s:9:\"Amsterdam\";s:6:\"\u0000*\u0000pub\";s:16:\"Elsevier Science\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Acceso mediante Istex
"O:16:\"UnpaywallOpenUrl\":35:{s:8:\"\u0000*\u0000email\";s:27:\"assistance-portail@inist.fr\";s:6:\"\u0000*\u0000fmt\";N;s:6:\"\u0000*\u0000doi\";s:29:\"10.1016\/S0022-0728(01)00411-9\";s:6:\"\u0000*\u0000pii\";N;s:7:\"\u0000*\u0000pmid\";N;s:9:\"\u0000*\u0000atitle\";N;s:9:\"\u0000*\u0000jtitle\";N;s:9:\"\u0000*\u0000stitle\";N;s:7:\"\u0000*\u0000date\";N;s:9:\"\u0000*\u0000volume\";N;s:8:\"\u0000*\u0000issue\";N;s:8:\"\u0000*\u0000spage\";N;s:8:\"\u0000*\u0000epage\";N;s:8:\"\u0000*\u0000pages\";N;s:7:\"\u0000*\u0000issn\";N;s:8:\"\u0000*\u0000eissn\";N;s:9:\"\u0000*\u0000aulast\";N;s:10:\"\u0000*\u0000aufirst\";N;s:9:\"\u0000*\u0000auinit\";N;s:10:\"\u0000*\u0000auinitm\";N;s:5:\"\u0000*\u0000au\";N;s:9:\"\u0000*\u0000aucorp\";N;s:7:\"\u0000*\u0000isbn\";N;s:8:\"\u0000*\u0000coden\";N;s:8:\"\u0000*\u0000genre\";N;s:7:\"\u0000*\u0000part\";N;s:9:\"\u0000*\u0000btitle\";N;s:8:\"\u0000*\u0000title\";N;s:8:\"\u0000*\u0000place\";N;s:6:\"\u0000*\u0000pub\";N;s:10:\"\u0000*\u0000edition\";N;s:9:\"\u0000*\u0000tpages\";N;s:9:\"\u0000*\u0000series\";N;s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";N;}"
Acceso mediante Unpaywall
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:29:\"10.1016\/S0022-0728(01)00411-9\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:9:\"\u0000*\u0000jtitle\";s:45:\"Journal of electroanalytical chemistry (1992)\";s:9:\"\u0000*\u0000stitle\";s:28:\"J. electroanal. chem. (1992)\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:3:\"507\";s:8:\"\u0000*\u0000issue\";s:3:\"1-2\";s:8:\"\u0000*\u0000spage\";s:2:\"89\";s:8:\"\u0000*\u0000epage\";s:2:\"95\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1572-6657\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"FEROCI\";s:10:\"\u0000*\u0000aufirst\";s:5:\"Marta\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"INESI, Achille\";i:1;s:14:\"ORSINI, Monica\";i:2;s:13:\"ROSSI, Leucio\";i:3;s:16:\"SOTGIU, Giovanni\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:38:\"New trends in organic electrochemistry\";s:8:\"\u0000*\u0000title\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:8:\"\u0000*\u0000place\";s:9:\"Amsterdam\";s:6:\"\u0000*\u0000pub\";s:16:\"Elsevier Science\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Acceso mediante Europe PubMed Central
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:29:\"10.1016\/S0022-0728(01)00411-9\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:9:\"\u0000*\u0000jtitle\";s:45:\"Journal of electroanalytical chemistry (1992)\";s:9:\"\u0000*\u0000stitle\";s:28:\"J. electroanal. chem. (1992)\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:3:\"507\";s:8:\"\u0000*\u0000issue\";s:3:\"1-2\";s:8:\"\u0000*\u0000spage\";s:2:\"89\";s:8:\"\u0000*\u0000epage\";s:2:\"95\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1572-6657\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"FEROCI\";s:10:\"\u0000*\u0000aufirst\";s:5:\"Marta\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"INESI, Achille\";i:1;s:14:\"ORSINI, Monica\";i:2;s:13:\"ROSSI, Leucio\";i:3;s:16:\"SOTGIU, Giovanni\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:38:\"New trends in organic electrochemistry\";s:8:\"\u0000*\u0000title\";s:132:\"An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with \u03b1, \u03b1'-di- and trichloroketones\";s:8:\"\u0000*\u0000place\";s:9:\"Amsterdam\";s:6:\"\u0000*\u0000pub\";s:16:\"Elsevier Science\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Acceso mediante arXiv
