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Journal Abstract Search
221 related items for PubMed ID: 16176903
1. A novel total synthesis of kinsenoside and goodyeroside A relying on the efficient reaction of the chiral 2(5H)-furanones. Zhang X, Huang HH, Chen QH. J Asian Nat Prod Res; 2005 Oct; 7(5):711-21. PubMed ID: 16176903 [Abstract] [Full Text] [Related]
2. Efficient synthesis of kinsenoside and goodyeroside a by a chemo-enzymatic approach. Zhang Y, Xia Y, Lai Y, Tang F, Luo Z, Xue Y, Yao G, Zhang Y, Zhang J. Molecules; 2014 Oct 22; 19(10):16950-8. PubMed ID: 25340300 [Abstract] [Full Text] [Related]
3. One-step preparation of O-(α-bromoacyl) cyanohydrins by minor enantiomer recycling: synthesis of 4-amino-2(5H)-furanones. Hertzberg R, Moberg C. J Org Chem; 2013 Sep 20; 78(18):9174-80. PubMed ID: 23980631 [Abstract] [Full Text] [Related]
4. Concise entry to chiral 5-(4-hydroxybutyl)-2(5H)-furanone via HTIB-mediated novel oxidative fragmentation: formal total synthesis of (+)-dubiusamine A. Kawasumi M, Iwabuchi Y. Org Lett; 2013 Apr 05; 15(7):1788-90. PubMed ID: 23530716 [Abstract] [Full Text] [Related]
5. Synthesis of combinatorial libraries of 3,4,5-trisubstituted 2(5H)-furanones. Part One: Construction of a sub-library of halogenated 5-alkoxy-2(5H)-furanones. Lattmann E, Billington DC, Langley CA. Drug Des Discov; 1999 Nov 05; 16(3):237-42. PubMed ID: 10624569 [Abstract] [Full Text] [Related]
6. Stereochemical study of chiral tautomeric flavorous furanones by vibrational circular dichroism. Yaguchi Y, Nakahashi A, Miura N, Sugimoto D, Monde K, Emura M. Org Lett; 2008 Nov 06; 10(21):4883-5. PubMed ID: 18817404 [Abstract] [Full Text] [Related]
7. Synthesis of nature product kinsenoside analogues with anti-inflammatory activity. Song W, Sun Y, Xu L, Sun Y, Li T, Peng P, Lou H. Bioorg Med Chem; 2021 Jan 01; 29():115854. PubMed ID: 33223464 [Abstract] [Full Text] [Related]
8. Design, synthesis and hepatoprotective activity of analogs of the natural product goodyeroside A. Zhang F, Han B, Li P, Lin Z, Yin D, Li Y, Zhong J, Huang H. Molecules; 2013 Feb 01; 18(2):1933-48. PubMed ID: 23377134 [Abstract] [Full Text] [Related]
9. Differential use of anhydropyranosides for enantiopure routes to bis-gamma-butyrolactones: a new approach to the frameworks of antibiotic and anticancer agents isoavenaciolide and ethisolide. Al-Tel TH, Al-Qawasmeh RA, Sabri SS, Voelter W. J Org Chem; 2009 Jul 03; 74(13):4690-6. PubMed ID: 19459653 [Abstract] [Full Text] [Related]
10. Efficient synthesis of 3-chloromethyl-2(5H)-furanones and 3-chloromethyl-5,6-dihydropyran-2-ones via the PdCl2-catalyzed chlorocyclocarbonylation of 2,3- or 3,4-allenols. Cheng X, Jiang X, Yu Y, Ma S. J Org Chem; 2008 Nov 21; 73(22):8960-5. PubMed ID: 18939873 [Abstract] [Full Text] [Related]
11. Synthesis of 2(3H)-furanones via electrophilic cyclization. Just ZW, Larock RC. J Org Chem; 2008 Apr 04; 73(7):2662-7. PubMed ID: 18321125 [Abstract] [Full Text] [Related]
12. Synthesis of combinatorial libraries of 3,4,5-trisubstituted 2(5H)-furanones. Part Two: Construction of a library of 4-amino-5-alkoxy-2(5H)-furanones. Lattmann E, Billington DC, Langley CA. Drug Des Discov; 1999 Nov 04; 16(3):243-50. PubMed ID: 10624570 [Abstract] [Full Text] [Related]
13. Total synthesis of (-)-orthodiffenes A and C. Liu J, Liu Y, Zhang X, Zhang C, Gao Y, Wang L, Du Y. J Org Chem; 2012 Nov 02; 77(21):9718-23. PubMed ID: 23051061 [Abstract] [Full Text] [Related]
14. A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure carba-D-ribofuranoses, carba-D-arabinofuranoses and carba-L-gulopyranose. Ghosh S, Bhaumik T, Sarkar N, Nayek A. J Org Chem; 2006 Dec 22; 71(26):9687-94. PubMed ID: 17168586 [Abstract] [Full Text] [Related]
15. Oxidative cleavage of 3-alkoxy-2,5-dihydrofurans and its application to the de novo synthesis of rare monosaccharides as exemplified by L-cymarose. Brasholz M, Reissig HU. Angew Chem Int Ed Engl; 2007 Dec 22; 46(10):1634-7. PubMed ID: 17219450 [No Abstract] [Full Text] [Related]
16. Stereoselective route to oxetanocin carbocyclic analogues based on a [2 + 2] photocycloaddition to a chiral 2(5H)-furanone. Rustullet A, Alibés R, de March P, Figueredo M, Font J. Org Lett; 2007 Jul 19; 9(15):2827-30. PubMed ID: 17583347 [Abstract] [Full Text] [Related]
17. Reactivity of gamma-hydroxy-alpha,beta-acetylenic esters with amines: facile synthesis of the optically active 4-amino-2(5H)-furanones. Zhou LH, Yu XQ, Pu L. J Org Chem; 2009 Mar 06; 74(5):2013-7. PubMed ID: 19195982 [Abstract] [Full Text] [Related]
18. Short synthesis of the seed germination inhibitor 3,4,5-trimethyl-2(5H)-furanone. Surmont R, Verniest G, De Kimpe N. J Org Chem; 2010 Aug 20; 75(16):5750-3. PubMed ID: 20704450 [Abstract] [Full Text] [Related]
19. Synthesis and preliminary bioactivity assays of 3,4-dichloro-5-(omega-hydroxyalkylamino)-2(5H)-furanones. Gondela E, Walczak KZ. Eur J Med Chem; 2010 Sep 20; 45(9):3993-7. PubMed ID: 20573426 [Abstract] [Full Text] [Related]
20. Stereoselective total synthesis of (+)-varitriol, (-)-varitriol, 5'-epi-(+)-varitriol, and 4'-epi-(-)-varitriol from D-mannitol. Ghosh S, Pradhan TK. J Org Chem; 2010 Mar 19; 75(6):2107-10. PubMed ID: 20180524 [Abstract] [Full Text] [Related] Page: [Next] [New Search]