NDLI: Alkaline Sodium Borohydride-Promoted Reductive Alkylation of β-Aminomercurials: Synthesis of 1,5-Functionalized Amines

Content Provider	Scilit
Author	Barluenga, José Campos, Pedro J. López-Prado, Joaquín Asensio, Gregorio
Copyright Year	1985
Description	ß-Aminoalkyl radicals generated by alkaline sodium borohydride reduction of aminomercurials react with electron-deficient olefins in an one pot procedure. These reactions allow direct synthesis of 5-aminonitriles and 5-aminoesters. 1,5-Diamines and aminoalcohols were also prepared by reduction of the former compounds.
Related Links	http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1985-31448.pdf
Ending Page	1129
Page Count	5
Starting Page	1125
ISSN	00397881
e-ISSN	1437210X
DOI	10.1055/s-1985-31448
Journal	Synthesis
Issue Number	12
Volume Number	1985
Language	English
Publisher	Georg Thieme Verlag KG
Publisher Date	1985-01-01
Access Restriction	Open
Subject Keyword	Journal: Synthesis Organic Chemistry Sodium Borohydride
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry Catalysis

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Alkaline Sodium Borohydride-Promoted Reductive Alkylation of β-Aminomercurials: Synthesis of 1,5-Functionalized Amines