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.
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| Formato: | JOUR |
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_09365214_v_n12_p1825_Nudelman |
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todo:paper_09365214_v_n12_p1825_Nudelman2023-10-03T15:48:37Z A highly convenient new methodology for the synthesis of N-nitrosamines from lithium amides Nudelman, N.S. Bonatti, A.E. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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 Nudelman, N.S. Bonatti, A.E. 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. |
| format |
JOUR |
| author |
Nudelman, N.S. Bonatti, A.E. |
| author_facet |
Nudelman, N.S. Bonatti, A.E. |
| author_sort |
Nudelman, N.S. |
| 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 |
| url |
http://hdl.handle.net/20.500.12110/paper_09365214_v_n12_p1825_Nudelman |
| work_keys_str_mv |
AT nudelmanns ahighlyconvenientnewmethodologyforthesynthesisofnnitrosaminesfromlithiumamides AT bonattiae ahighlyconvenientnewmethodologyforthesynthesisofnnitrosaminesfromlithiumamides AT nudelmanns highlyconvenientnewmethodologyforthesynthesisofnnitrosaminesfromlithiumamides AT bonattiae highlyconvenientnewmethodologyforthesynthesisofnnitrosaminesfromlithiumamides |
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