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182 related items for PubMed ID: 18489153
1. Regioselective synthesis and structural studies of substituted gamma-hydroxybutenolides with use of a tandem Baylis-Hillman/singlet oxygenation reaction. Patil SN, Liu F. J Org Chem; 2008 Jun 20; 73(12):4476-83. PubMed ID: 18489153 [Abstract] [Full Text] [Related]
2. Fluoride-assisted regioselective conversion of functionalized furans to alpha-substituted gamma-hydroxybutenolides using singlet oxygen. Patil SN, Liu F. J Org Chem; 2007 Aug 03; 72(16):6305-8. PubMed ID: 17629339 [Abstract] [Full Text] [Related]
3. Base-assisted regio- and diastereoselective conversion of functionalized furans to butenolides using singlet oxygen. Patil SN, Liu F. Org Lett; 2007 Jan 18; 9(2):195-8. PubMed ID: 17217263 [Abstract] [Full Text] [Related]
4. Synthesis of (+)-zerumin B using a regioselective singlet oxygen furan oxidation. Margaros I, Vassilikogiannakis G. J Org Chem; 2008 Mar 07; 73(5):2021-3. PubMed ID: 18247492 [Abstract] [Full Text] [Related]
5. Diversely substituted sugar-linked alpha,beta-unsaturated gamma-lactones from sugar-derived Baylis-Hillman adducts via a RCM. Krishna PR, Narsingam M. J Comb Chem; 2007 Mar 07; 9(1):62-9. PubMed ID: 17206833 [Abstract] [Full Text] [Related]
6. Regioselective entry to bromo-gamma-hydroxybutenolides: useful building blocks for assemblying natural product-like libraries. Aquino M, Bruno I, Riccio R, Gomez-Paloma L. Org Lett; 2006 Oct 12; 8(21):4831-4. PubMed ID: 17020314 [Abstract] [Full Text] [Related]
7. First asymmetric synthesis of chiral beta-iodo Baylis-Hillman esters via tandem 1,4-conjugate addition/carbonyl coupling reactions. Xu X, Chen D, Wei HX, Li G, Xiao TL, Armstrong DW. Chirality; 2003 Feb 12; 15(2):139-42. PubMed ID: 12520505 [Abstract] [Full Text] [Related]
8. Phosphonylpyrazoles from Bestmann-Ohira reagent and nitroalkenes: synthesis and dynamic NMR studies. Muruganantham R, Namboothiri I. J Org Chem; 2010 Apr 02; 75(7):2197-205. PubMed ID: 20218559 [Abstract] [Full Text] [Related]
9. Construction of chiral quaternary carbon through Morita-Baylis-Hillman reaction: an enantioselective approach to 3-substituted 3-hydroxyoxindole derivatives. Guan XY, Wei Y, Shi M. Chemistry; 2010 Dec 10; 16(46):13617-21. PubMed ID: 21104713 [No Abstract] [Full Text] [Related]
10. Illustrating the power of singlet oxygen chemistry in a synthetic context: biomimetic syntheses of litseaverticillols A-G, I and J and the structural reassignment of litseaverticillol E. Vassilikogiannakis G, Margaros I, Montagnon T, Stratakis M. Chemistry; 2005 Oct 07; 11(20):5899-907. PubMed ID: 15971279 [Abstract] [Full Text] [Related]
11. Synthesis of a versatile (S)-3-(hydroxymethyl)butane-1,2,4-triol building block and its application for the stereoselective synthesis of N-homoceramides. Hillaert U, Van Calenbergh S. Org Lett; 2005 Dec 22; 7(26):5769-72. PubMed ID: 16354062 [Abstract] [Full Text] [Related]
12. Sequential aza-Baylis-Hillman/ring closing metathesis/aromatization as a novel route for the synthesis of substituted pyrroles. Declerck V, Ribière P, Martinez J, Lamaty F. J Org Chem; 2004 Nov 26; 69(24):8372-81. PubMed ID: 15549809 [Abstract] [Full Text] [Related]
13. Diastereoselective synthesis of delta-aminoacids through domino Ireland-Claisen rearrangement and Michael addition. Garrido NM, García M, Díez D, Sánchez MR, Sanz F, Urones JG. Org Lett; 2008 May 01; 10(9):1687-90. PubMed ID: 18399652 [Abstract] [Full Text] [Related]
14. Reactions of iminium ions with Michael acceptors through a Morita-Baylis-Hillman-type reaction: enantiocontrol and applications in synthesis. Myers EL, de Vries JG, Aggarwal VK. Angew Chem Int Ed Engl; 2007 May 01; 46(11):1893-6. PubMed ID: 17278162 [No Abstract] [Full Text] [Related]
15. Baylis-Hillman reaction assisted parallel synthesis of 3,5-disubstituted isoxazoles and their in vivo bioevaluation as antithrombotic agents. Batra S, Roy AK, Patra A, Bhaduri AP, Surin WR, Raghavan SA, Sharma P, Kapoor K, Dikshit M. Bioorg Med Chem; 2004 May 01; 12(9):2059-77. PubMed ID: 15080910 [Abstract] [Full Text] [Related]
16. C10-substituted camphors and fenchones by electrophilic treatment of 2-methylenenorbornan-1-ols: enantiospecificity, scope, and limitations. de la Moya Cerero S, García Martínez A, Teso Vilar E, García Fraile A, Lora Maroto B. J Org Chem; 2003 Feb 21; 68(4):1451-8. PubMed ID: 12585887 [Abstract] [Full Text] [Related]
18. "Diversity oriented synthesis" of functionalized chiral tetrahydropyridines: potential GABA receptor agonists and azasugars from natural amino acids via a sequential Baylis-Hillman reaction and RCM protocol. Krishna PR, Reddy PS. J Comb Chem; 2008 Feb 21; 10(3):426-35. PubMed ID: 18410150 [Abstract] [Full Text] [Related]
19. Efficient Baylis-Hillman reactions of cyclic enones in methanol as catalyzed by methoxide anion. Luo S, Mi X, Xu H, Wang PG, Cheng JP. J Org Chem; 2004 Nov 26; 69(24):8413-22. PubMed ID: 15549815 [Abstract] [Full Text] [Related]
20. Stereoselective synthesis of 3-oxygenated-cis-dialkyl-2,5-substituted tetrahydrofurans from cyclohexadienediols. Brovetto M, Seoane G. J Org Chem; 2008 Aug 01; 73(15):5776-85. PubMed ID: 18582114 [Abstract] [Full Text] [Related] Page: [Next] [New Search]