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223 related items for PubMed ID: 25675109
1. Construction of chiral α-amino quaternary stereogenic centers via phase-transfer catalyzed enantioselective α-alkylation of α-amidomalonates. Ha MW, Lee M, Choi S, Kim S, Hong S, Park Y, Kim MH, Kim TS, Lee J, Lee JK, Park HG. J Org Chem; 2015 Mar 20; 80(6):3270-9. PubMed ID: 25675109 [Abstract] [Full Text] [Related]
2. Enantioselective Synthesis of Chiral α-Azido and α-Aryloxy Quaternary Stereogenic Centers via the Phase-Transfer-Catalyzed α-Alkylation of α-Bromomalonates, Followed by SN2 Substitution. Kim D, Ha MW, Hong S, Park C, Kim B, Yang J, Park HG. J Org Chem; 2017 May 05; 82(9):4936-4943. PubMed ID: 28414466 [Abstract] [Full Text] [Related]
3. Enantioselective Synthesis of Chiral α-Thio-Quaternary Stereogenic Centers via Phase-Transfer-Catalyzed α-Alkylation of α-Acylthiomalonates. Ha MW, Lee JY, Kim D, Lee G, Lee JK, Hong S, Park HG. J Org Chem; 2018 Jan 19; 83(2):1011-1018. PubMed ID: 29262254 [Abstract] [Full Text] [Related]
4. Highly enantioselective synthesis of α,α-dialkylmalonates by phase-transfer catalytic desymmetrization. Hong S, Lee J, Kim M, Park Y, Park C, Kim MH, Jew SS, Park HG. J Am Chem Soc; 2011 Apr 06; 133(13):4924-9. PubMed ID: 21388212 [Abstract] [Full Text] [Related]
5. Enantioselective synthesis of α-halo-α-alkylmalonates via phase-transfer catalytic α-alkylation. Hong S, Kim M, Jung M, Ha MW, Lee M, Park Y, Kim MH, Kim TS, Lee J, Park HG. Org Biomol Chem; 2014 Mar 07; 12(9):1510-7. PubMed ID: 24448720 [Abstract] [Full Text] [Related]
6. Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates. Ha MW, Hong S, Park C, Park Y, Lee J, Kim MH, Lee J, Park HG. Org Biomol Chem; 2013 Jun 28; 11(24):4030-9. PubMed ID: 23666205 [Abstract] [Full Text] [Related]
8. The highly enantioselective phase-transfer catalytic mono-alkylation of malonamic esters. Kim MH, Choi SH, Lee YJ, Lee J, Nahm K, Jeong BS, Park HG, Jew SS. Chem Commun (Camb); 2009 Feb 21; (7):782-4. PubMed ID: 19322440 [Abstract] [Full Text] [Related]
10. Catalytic enantioselective alkylations of tetrasubstituted olefins. Synthesis of all-carbon quaternary stereogenic centers through Cu-catalyzed asymmetric conjugate additions of alkylzinc reagents to enones. Hird AW, Hoveyda AH. J Am Chem Soc; 2005 Nov 02; 127(43):14988-9. PubMed ID: 16248613 [Abstract] [Full Text] [Related]
11. Catalytic asymmetric alkylations of ketoimines. Enantioselective synthesis of N-substituted quaternary carbon stereogenic centers by Zr-catalyzed additions of dialkylzinc reagents to aryl-, alkyl-, and trifluoroalkyl-substituted ketoimines. Fu P, Snapper ML, Hoveyda AH. J Am Chem Soc; 2008 Apr 23; 130(16):5530-41. PubMed ID: 18376838 [Abstract] [Full Text] [Related]
12. Highly enantioselective synthesis of (S)-alpha-alkyl-alpha,beta-diaminopropionic acids via asymmetric phase-transfer catalytic alkylation of 2-phenyl-2-imidazoline-4-carboxylic acid tert-butyl esters. Park Y, Kang S, Lee YJ, Kim TS, Jeong BS, Park HG, Jew SS. Org Lett; 2009 Aug 20; 11(16):3738-41. PubMed ID: 19634890 [Abstract] [Full Text] [Related]
18. Asymmetric Synthesis of α-Quaternary γ-Lactams through Palladium-Catalyzed Asymmetric Allylic Alkylation. Song T, Arseniyadis S, Cossy J. Org Lett; 2019 Feb 01; 21(3):603-607. PubMed ID: 30645137 [Abstract] [Full Text] [Related]
19. Enantioselective Friedel-Crafts alkylation of indoles with trifluoroethylidene malonates by copper-bis(oxazoline) complexes: construction of trifluoromethyl-substituted stereogenic tertiary carbon center. Wen L, Shen Q, Wan X, Lu L. J Org Chem; 2011 Apr 01; 76(7):2282-5. PubMed ID: 21375277 [Abstract] [Full Text] [Related]