Literature DB >> 19591453

Secondary amine formation from reductive amination of carbonyl compounds promoted by Lewis acid using the InCl3/Et3SiH system.

On-Yi Lee1, Ka-Lun Law, Dan Yang.   

Abstract

A robust and reliable method has been developed for reductive amination of primary amines with various aldehydes and ketones using Zn(ClO(4))(2) x 6 H(2)O as a catalyst. [In-H] generated in situ via a combination of InCl(3) and Et(3)SiH is employed as an effective reducing system. A variety of secondary amines can be synthesized in a one-pot procedure in excellent yields.

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Year:  2009        PMID: 19591453     DOI: 10.1021/ol901111g

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Catalytic acceptorless dehydrogenations: Ru-Macho catalyzed construction of amides and imines.

Authors:  Nathan J Oldenhuis; Vy M Dong; Zhibin Guan
Journal:  Tetrahedron       Date:  2014-07-08       Impact factor: 2.457

2.  Relationship between Structure and Antibacterial Activity of α-Aminophosphonate Derivatives Obtained via Lipase-Catalyzed Kabachnik-Fields Reaction.

Authors:  Dominik Koszelewski; Paweł Kowalczyk; Paweł Śmigielski; Jan Samsonowicz-Górski; Karol Kramkowski; Aleksandra Wypych; Mateusz Szymczak; Ryszard Ostaszewski
Journal:  Materials (Basel)       Date:  2022-05-27       Impact factor: 3.748

3.  Highly functionalized 1,2-diamino compounds through reductive amination of amino acid-derived β-keto esters.

Authors:  Paula Pérez-Faginas; M Teresa Aranda; M Teresa García-López; Lourdes Infantes; Asia Fernández-Carvajal; José Manuel González-Ros; Antonio Ferrer-Montiel; Rosario González-Muñiz
Journal:  PLoS One       Date:  2013-01-07       Impact factor: 3.240

4.  Palladium-catalyzed reductive coupling of phenols with anilines and amines: efficient conversion of phenolic lignin model monomers and analogues to cyclohexylamines.

Authors:  Zhengwang Chen; Huiying Zeng; Hang Gong; Haining Wang; Chao-Jun Li
Journal:  Chem Sci       Date:  2015-04-30       Impact factor: 9.825

  4 in total

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