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Direct Activation of the C(sp3)-NH2 Bond of Primary Aliphatic Alkylamines by a High-Valent CoIII,IV2(µ-O)2 Diamond Core Complex.
Li, Yan; Handunneththige, Suhashini; Xiong, Jin; Guo, Yisong; Talipov, Marat R; Wang, Dong.
Afiliación
  • Li Y; Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Dynamics, University of Montana, Missoula, Montana 59812, United States.
  • Handunneththige S; Department of Chemistry and Biochemistry, New Mexico State University, Las Cruces, New Mexico 88003, United States.
  • Xiong J; Department of Chemistry, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
  • Guo Y; Department of Chemistry, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
  • Talipov MR; Department of Chemistry and Biochemistry, New Mexico State University, Las Cruces, New Mexico 88003, United States.
  • Wang D; Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Dynamics, University of Montana, Missoula, Montana 59812, United States.
J Am Chem Soc ; 145(4): 2690-2697, 2023 Feb 01.
Article en En | MEDLINE | ID: mdl-36689463
ABSTRACT
Aliphatic alkylamines are abundant feedstock and versatile building blocks for many organic transformations. While remarkable progress has been made to construct C-N bonds on aliphatic and aromatic carbon centers, the activation and functionalization of C(sp3)-NH2 bonds in primary alkylamines remain a challenging process. In the present work, we discovered an unprecedented method to directly activate the C(sp3)-NH2 bond of primary alkylamines by a high-valent dinuclear CoIII,IV2(µ-O)2 diamond core complex. This reaction results in the installation of other functional groups such as halides and alkenes onto the α-carbon center concomitant with the 2-e- oxidation of the nitrogen atom on the amino group to form NH2OH. These results shed light on future development enabling versatile functionalization of primary alkylamines based on the dinuclear cobalt system. Moreover, our work suggests that a related high-valent copper-oxo intermediate is likely generated in the ammonia monooxygenase catalytic cycle to affect the oxidation of NH3 to NH2OH.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos