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Reductive opening of a cyclopropane ring in the Ni(II) coordination environment: a route to functionalized dehydroalanine and cysteine derivatives

The involvement of an α,α-cyclopropanated amino acid in the chiral Ni(II) coordination environment in the form of a Schiff base is considered as a route to electrochemical broadening of the donor–acceptor cyclopropane concept in combination with chirality induction in the targeted products. A tenden...

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Detalles Bibliográficos
Autores principales: Levitskiy, Oleg A, Aglamazova, Olga I, Grishin, Yuri K, Magdesieva, Tatiana V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475196/
https://www.ncbi.nlm.nih.gov/pubmed/36128429
http://dx.doi.org/10.3762/bjoc.18.121

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