New route for 1-substituted hydantoins
- Autores
- Orazi, Orfeo Osvaldo; Corral, Renée Antonio
- Año de publicación
- 1965
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Alkytation reactions on hydantoins (I) lead smoothly to 3-alkyl derivatives; more rigorous conditions allow further substitution at position 1 provided the N1-H group is activated by an aryl group or an ethylenic bond attached to the adjacent C52,a. All the hitherto available methods for the not readily accessible 3-unsubstituted-1-alkylhydantoins (IV) require placing the substituent at the appropriate nitrogen atom prior to the complete formation of the hydantoin system.
Facultad de Ciencias Exactas - Materia
-
Química
Hidantoínas - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/134790
Ver los metadatos del registro completo
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New route for 1-substituted hydantoinsOrazi, Orfeo OsvaldoCorral, Renée AntonioQuímicaHidantoínasAlkytation reactions on hydantoins (I) lead smoothly to 3-alkyl derivatives; more rigorous conditions allow further substitution at position 1 provided the N1-H group is activated by an aryl group or an ethylenic bond attached to the adjacent C52,a. All the hitherto available methods for the not readily accessible 3-unsubstituted-1-alkylhydantoins (IV) require placing the substituent at the appropriate nitrogen atom prior to the complete formation of the hydantoin system.Facultad de Ciencias Exactas1965-09-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf508-508http://sedici.unlp.edu.ar/handle/10915/134790enginfo:eu-repo/semantics/altIdentifier/issn/0014-4754info:eu-repo/semantics/altIdentifier/issn/1420-9071info:eu-repo/semantics/altIdentifier/issn/1420-682Xinfo:eu-repo/semantics/altIdentifier/doi/10.1007/bf02138960info:eu-repo/semantics/altIdentifier/pmid/5872608info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:32:22Zoai:sedici.unlp.edu.ar:10915/134790Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:32:23.17SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
New route for 1-substituted hydantoins |
| title |
New route for 1-substituted hydantoins |
| spellingShingle |
New route for 1-substituted hydantoins Orazi, Orfeo Osvaldo Química Hidantoínas |
| title_short |
New route for 1-substituted hydantoins |
| title_full |
New route for 1-substituted hydantoins |
| title_fullStr |
New route for 1-substituted hydantoins |
| title_full_unstemmed |
New route for 1-substituted hydantoins |
| title_sort |
New route for 1-substituted hydantoins |
| dc.creator.none.fl_str_mv |
Orazi, Orfeo Osvaldo Corral, Renée Antonio |
| author |
Orazi, Orfeo Osvaldo |
| author_facet |
Orazi, Orfeo Osvaldo Corral, Renée Antonio |
| author_role |
author |
| author2 |
Corral, Renée Antonio |
| author2_role |
author |
| dc.subject.none.fl_str_mv |
Química Hidantoínas |
| topic |
Química Hidantoínas |
| dc.description.none.fl_txt_mv |
Alkytation reactions on hydantoins (I) lead smoothly to 3-alkyl derivatives; more rigorous conditions allow further substitution at position 1 provided the N1-H group is activated by an aryl group or an ethylenic bond attached to the adjacent C52,a. All the hitherto available methods for the not readily accessible 3-unsubstituted-1-alkylhydantoins (IV) require placing the substituent at the appropriate nitrogen atom prior to the complete formation of the hydantoin system. Facultad de Ciencias Exactas |
| description |
Alkytation reactions on hydantoins (I) lead smoothly to 3-alkyl derivatives; more rigorous conditions allow further substitution at position 1 provided the N1-H group is activated by an aryl group or an ethylenic bond attached to the adjacent C52,a. All the hitherto available methods for the not readily accessible 3-unsubstituted-1-alkylhydantoins (IV) require placing the substituent at the appropriate nitrogen atom prior to the complete formation of the hydantoin system. |
| publishDate |
1965 |
| dc.date.none.fl_str_mv |
1965-09-15 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://sedici.unlp.edu.ar/handle/10915/134790 |
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http://sedici.unlp.edu.ar/handle/10915/134790 |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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openAccess |
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