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Journal Abstract Search
543 related items for PubMed ID: 32729851
41. One-pot Reductive Amination of carbonyl Compounds with Nitro Compounds by Transfer Hydrogenation over Co-Nx as catalyst. Zhou P, Zhang Z. ChemSusChem; 2017 May 09; 10(9):1892-1897. PubMed ID: 28345301 [Abstract] [Full Text] [Related]
42. Amine dehydrogenases: efficient biocatalysts for the reductive amination of carbonyl compounds. Knaus T, Böhmer W, Mutti FG. Green Chem; 2017 Jan 21; 19(2):453-463. PubMed ID: 28663713 [Abstract] [Full Text] [Related]
43. Advances in the Catalytic Reductive Amination of Furfural to Furfural Amine: The Momentous Role of Active Metal Sites. Saini MK, Kumar S, Li H, Babu SA, Saravanamurugan S. ChemSusChem; 2022 Apr 07; 15(7):e202200107. PubMed ID: 35171526 [Abstract] [Full Text] [Related]
44. Nitrogen-Doped Carbon-Supported Nickel Nanoparticles: A Robust Catalyst to Bridge the Hydrogenation of Nitriles and the Reductive Amination of Carbonyl Compounds for the Synthesis of Primary Amines. Zhang Y, Yang H, Chi Q, Zhang Z. ChemSusChem; 2019 Mar 21; 12(6):1246-1255. PubMed ID: 30600939 [Abstract] [Full Text] [Related]
45. Chemoselective Reductive Amination of Carbonyl Compounds for the Synthesis of Tertiary Amines Using SnCl2·2H2O/PMHS/MeOH. Nayal OS, Bhatt V, Sharma S, Kumar N. J Org Chem; 2015 Jun 05; 80(11):5912-8. PubMed ID: 25938581 [Abstract] [Full Text] [Related]
56. Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane. Gautier FM, Jones S, Li X, Martin SJ. Org Biomol Chem; 2011 Oct 26; 9(22):7860-8. PubMed ID: 21960353 [Abstract] [Full Text] [Related]
57. Selective N-alkylation of amines using nitriles under hydrogenation conditions: facile synthesis of secondary and tertiary amines. Ikawa T, Fujita Y, Mizusaki T, Betsuin S, Takamatsu H, Maegawa T, Monguchi Y, Sajiki H. Org Biomol Chem; 2012 Jan 14; 10(2):293-304. PubMed ID: 22068239 [Abstract] [Full Text] [Related]
58. N-Dimethylation and N-Functionalization of Amines Using Ru Nanoparticle Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source. Liu J, Song Y, Wu X, Ma L. ACS Omega; 2021 Sep 07; 6(35):22504-22513. PubMed ID: 34514223 [Abstract] [Full Text] [Related]