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Journal Abstract Search
265 related items for PubMed ID: 31162782
1. Transition-Metal-Free Hydrogen Autotransfer: Diastereoselective N-Alkylation of Amines with Racemic Alcohols. Xiao M, Yue X, Xu R, Tang W, Xue D, Li C, Lei M, Xiao J, Wang C. Angew Chem Int Ed Engl; 2019 Jul 29; 58(31):10528-10536. PubMed ID: 31162782 [Abstract] [Full Text] [Related]
2. From racemic alcohols to enantiopure amines: Ru-catalyzed diastereoselective amination. Oldenhuis NJ, Dong VM, Guan Z. J Am Chem Soc; 2014 Sep 10; 136(36):12548-51. PubMed ID: 25170560 [Abstract] [Full Text] [Related]
3. N-Alkylation by Hydrogen Autotransfer Reactions [corrected]. Ma X, Su C, Xu Q. Top Curr Chem (Cham); 2016 Jun 10; 374(3):27. PubMed ID: 27573267 [Abstract] [Full Text] [Related]
4. Discovery and mechanistic studies of a general air-promoted metal-catalyzed aerobic N-alkylation reaction of amides and amines with alcohols. Liu C, Liao S, Li Q, Feng S, Sun Q, Yu X, Xu Q. J Org Chem; 2011 Jul 15; 76(14):5759-73. PubMed ID: 21657274 [Abstract] [Full Text] [Related]
5. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines. Lin GQ, Xu MH, Zhong YW, Sun XW. Acc Chem Res; 2008 Jul 15; 41(7):831-40. PubMed ID: 18533688 [Abstract] [Full Text] [Related]
7. Iridium-catalyzed diastereoselective amination of alcohols with chiral tert-butanesulfinamide by the use of a borrowing hydrogen methodology. Xi X, Li Y, Wang G, Xu G, Shang L, Zhang Y, Xia L. Org Biomol Chem; 2019 Sep 07; 17(33):7651-7654. PubMed ID: 31353383 [Abstract] [Full Text] [Related]
9. General Synthesis of N-Alkylation of Amines with Secondary Alcohols via Hydrogen Autotransfer. Subaramanian M, Midya SP, Ramar PM, Balaraman E. Org Lett; 2019 Nov 15; 21(22):8899-8903. PubMed ID: 31691555 [Abstract] [Full Text] [Related]
19. C-Alkylation of Secondary Alcohols by Primary Alcohols through Manganese-Catalyzed Double Hydrogen Autotransfer. El-Sepelgy O, Matador E, Brzozowska A, Rueping M. ChemSusChem; 2019 Jul 05; 12(13):3099-3102. PubMed ID: 30239145 [Abstract] [Full Text] [Related]