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Título

Organocatalytic transfer hydrogenation and hydrosilylation reactions

AutorHerrera, Raquel P. CSIC ORCID
Palabras claveLewis bases
Thioureas
Aminocatalysis
Organocatalysis
Hydrosilylation
Phosphoric acid
Trichlorosilane
Reduction
Hantzsch ester
Transfer hydrogenation
Fecha de publicación2016
EditorSpringer Nature
CitaciónTopics in Current Chemistry 374: 29 (2016)
ResumenThe reduction of different carbon–carbon or carbon–heteroatom double bonds is a powerful tool that generates in many cases new stereogenic centers. In the last decade, the organocatalytic version of these transformations has attracted more attention, and remarkable progress has been made in this way. Organocatalysts such as chiral Brønsted acids, thioureas, chiral secondary amines or Lewis bases have been successfully used for this purpose. In this context, this chapter will cover pioneering and seminal examples using Hantzsch dihydropyridines 1 and trichlorosilane 2 as reducing agents. More recent examples will be also cited in order to cover as much as possible the complete research in this field.
DescripciónThis article is part of the Topical Collection ‘‘Hydrogen Transfer Reactions’’.
Versión del editorhttps://doi.org/10.1007/s41061-016-0032-4
URIhttp://hdl.handle.net/10261/154919
DOI10.1007/s41061-016-0032-4
Identificadoresdoi: 10.1007/s41061-016-0032-4
issn: 2365-0869
e-issn: 2364-8961
Aparece en las colecciones: (ISQCH) Artículos




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