A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides
N-nitrosoalkylamines were efficiently synthesized from the reaction of lithium amides with NO at atmospheric pressure using dialkylamines as starting materials. With asymmetric amines stereoselectivity is observed giving rise to different amounts of E and Z isomers.
Guardado en:
| Publicado: |
2000
|
|---|---|
| Materias: | |
| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09365214_v_n12_p1825_Nudelman http://hdl.handle.net/20.500.12110/paper_09365214_v_n12_p1825_Nudelman |
| Aporte de: |
| id |
paper:paper_09365214_v_n12_p1825_Nudelman |
|---|---|
| record_format |
dspace |
| spelling |
paper:paper_09365214_v_n12_p1825_Nudelman2023-06-08T15:53:16Z A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides Alkyl nitrosamines Lithium amides Nitrosamines Nitrosation NO reactivity amide lithium nitric oxide nitrosamine article atmospheric pressure chemical reaction methodology nitrosation stereochemistry synthesis N-nitrosoalkylamines were efficiently synthesized from the reaction of lithium amides with NO at atmospheric pressure using dialkylamines as starting materials. With asymmetric amines stereoselectivity is observed giving rise to different amounts of E and Z isomers. 2000 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09365214_v_n12_p1825_Nudelman http://hdl.handle.net/20.500.12110/paper_09365214_v_n12_p1825_Nudelman |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Alkyl nitrosamines Lithium amides Nitrosamines Nitrosation NO reactivity amide lithium nitric oxide nitrosamine article atmospheric pressure chemical reaction methodology nitrosation stereochemistry synthesis |
| spellingShingle |
Alkyl nitrosamines Lithium amides Nitrosamines Nitrosation NO reactivity amide lithium nitric oxide nitrosamine article atmospheric pressure chemical reaction methodology nitrosation stereochemistry synthesis A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| topic_facet |
Alkyl nitrosamines Lithium amides Nitrosamines Nitrosation NO reactivity amide lithium nitric oxide nitrosamine article atmospheric pressure chemical reaction methodology nitrosation stereochemistry synthesis |
| description |
N-nitrosoalkylamines were efficiently synthesized from the reaction of lithium amides with NO at atmospheric pressure using dialkylamines as starting materials. With asymmetric amines stereoselectivity is observed giving rise to different amounts of E and Z isomers. |
| title |
A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| title_short |
A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| title_full |
A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| title_fullStr |
A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| title_full_unstemmed |
A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides |
| title_sort |
highly convenient new methodology for the synthesis of n-nitrosamines from lithium amides |
| publishDate |
2000 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09365214_v_n12_p1825_Nudelman http://hdl.handle.net/20.500.12110/paper_09365214_v_n12_p1825_Nudelman |
| _version_ |
1768546308524605440 |