Prolinethiol ether catalysis in an asymmetric Michael reaction: solvent-free synthesis of functionalized monohaloalkenes.
暂无分享,去创建一个
Zhen-yuan Xu | Yifeng Wang | Danqian Xu | Chao Wu | Xiao-hua Du | Ai-Bao Xia | Zhaobo Li
[1] Zhen-yuan Xu,et al. Organocatalytic Diels-Alder reactions catalysed by supramolecular self-assemblies formed from chiral amines and poly(alkene glycol)s. , 2012, Chemistry.
[2] E. Negishi,et al. Highly(≥98%) Stereo- and Regioselective Trisubstituted Alkene Synthesis of Wide Applicability via 1-Halo-1-alkyne Hydroboration-Tandem Negishi-Suzuki Coupling or Organoborate Migratory Insertion Protocol. , 2011, Advanced synthesis & catalysis.
[3] K. Jørgensen,et al. A simple recipe for sophisticated cocktails: organocatalytic one-pot reactions--concept, nomenclature, and future perspectives. , 2011, Angewandte Chemie.
[4] P. Helquist,et al. Concise, convergent syntheses of (±)-trichostatin A utilizing a Pd-catalyzed ketone enolate α-alkenylation reaction. , 2011, Organic letters.
[5] A. Moyano,et al. Asymmetric organocatalytic cyclization and cycloaddition reactions. , 2011, Chemical reviews.
[6] Carmen Concellón,et al. Direct aldol reactions catalyzed by a heterogeneous guanidinium salt/proline system under solvent-free conditions. , 2011, Organic letters.
[7] M. Nielsen,et al. Asymmetric organocatalytic monofluorovinylations. , 2011, Journal of the American Chemical Society.
[8] Dacheng Li,et al. TBAF-mediated reactions of 1,1-dibromo-1-alkenes with thiols and amines and regioselective synthesis of 1,2-heterodisubstituted alkenes. , 2011, The Journal of organic chemistry.
[9] M. Bennasar,et al. A straightforward synthetic entry to cleavamine-type indole alkaloids by a ring-closing metathesis-vinyl halide Heck cyclization strategy. , 2011, Organic letters.
[10] Shih-Hsiung Wu,et al. Synthesis and biological evaluation of polyenylpyrrole derivatives as anticancer agents acting through caspases-dependent apoptosis. , 2010, Journal of medicinal chemistry.
[11] Lei Wang,et al. Sugar-Based Pyrrolidine as a Highly Enantioselective Organocatalyst for Asymmetric Michael Addition of Ketones to Nitrostyrenes , 2010 .
[12] Danqian Xu,et al. The highly enantioselective Michael addition of ketones to nitrodienes catalyzed by the efficient organocatalyst system of pyrrolidinyl-thioimidazole and chiral thioureido acid. , 2010, Organic & biomolecular chemistry.
[13] Xiaodong Shi,et al. Efficient synthesis of E-alpha-haloenones through chemoselective alkyne activation over allene with triazole-Au catalysts. , 2010, Organic letters.
[14] Jie Tang,et al. Dual organocatalytic ion-pair assemblies: a highly efficient approach for the enantioselective oxa-Michael-mannich reaction of salicylic aldehydes with cyclohexenones. , 2010, Chemistry.
[15] K. Jørgensen,et al. Organocatalysis--after the gold rush. , 2009, Chemical Society reviews.
[16] L. Crovetto,et al. Highly enantio- and diastereoselective organocatalytic desymmetrization of prochiral cyclohexanones by simple direct aldol reaction catalyzed by proline. , 2009, Chemistry.
[17] B. Marciniec,et al. New one-pot synthesis of (E)-beta-aryl vinyl halides from styrenes. , 2009, Organic letters.
[18] Jie Tang,et al. In situ enamine activation in aqueous salt solutions: highly efficient asymmetric organocatalytic Diels-Alder reaction of cyclohexenones with nitroolefins. , 2009, Angewandte Chemie.
[19] Yunpeng Lu,et al. Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins. , 2009, Organic letters.
[20] J. Mousseau,et al. Convenient one-pot synthesis of (E)-beta-aryl vinyl halides from benzyl bromides and dihalomethanes. , 2008, Organic letters.
[21] R. SanMartin,et al. A nonsymmetric pincer-catalyzed Suzuki-Miyaura arylation of benzyl halides and other nonactivated unusual coupling partners. , 2008, The Journal of organic chemistry.
[22] D. MacMillan,et al. The advent and development of organocatalysis , 2008, Nature.
[23] A. Alexakis,et al. Enantioselective organocatalytic conjugate addition of aldehydes to nitrodienes. , 2008, Organic letters.
[24] G. Guillena,et al. A highly efficient solvent-free asymmetric direct aldol reaction organocatalyzed by recoverable (S)-binam-L-prolinamides. ESI-MS evidence of the enamine-iminium formation. , 2008, The Journal of organic chemistry.
[25] J. Verkade,et al. (t-Bu)2PN=P(i-BuNCH2CH2)3N: new efficient ligand for palladium-catalyzed C-N couplings of aryl and heteroaryl bromides and chlorides and for vinyl bromides at room temperature. , 2008, The Journal of organic chemistry.
[26] S. Mukherjee,et al. Asymmetric enamine catalysis. , 2007, Chemical reviews.
[27] E. De Clercq,et al. Synthesis and antiviral evaluation of 6-(alkyl-heteroaryl)furo[2,3-d]pyrimidin-2(3H)-one nucleosides and analogues with ethynyl, ethenyl, and ethyl spacers at C6 of the furopyrimidine core. , 2007, Journal of medicinal chemistry.
[28] Yewen Fang,et al. Preference of 4-exo ring closure in copper-catalyzed intramolecular coupling of vinyl bromides with alcohols. , 2007, Journal of the American Chemical Society.
[29] R. S. Coleman,et al. Total synthesis of gymnoconjugatins A and B. , 2006, The Journal of organic chemistry.
[30] Armando Carlone,et al. A simple asymmetric organocatalytic approach to optically active cyclohexenones. , 2006, Chemical communications.
[31] Jung Woon Yang,et al. The Organic Approach to Asymmetric Catalysis , 2006, Science.
[32] Marie-Eve Lebrun,et al. Stereoselective synthesis of Z alkenyl halides via Julia olefination. , 2006, The Journal of organic chemistry.
[33] B. Trost,et al. Divergent enantioselective synthesis of (-)-galanthamine and (-)-morphine. , 2005, Journal of the American Chemical Society.
[34] F. Felpin. Practical and efficient Suzuki-Miyaura cross-coupling of 2-iodocycloenones with arylboronic acids catalyzed by recyclable Pd(0)/C. , 2005, The Journal of organic chemistry.
[35] Koichi Tanaka,et al. Solvent-free Organic Synthesis: TANAKA/SOLV.FREE ORG.SYNT O-BK , 2005 .
[36] A. Alexakis,et al. The Use of N‐Alkyl‐2,2′‐bipyrrolidine Derivatives as Organocatalysts for the Asymmetric Michael Addition of Ketones and Aldehydes to Nitroolefins , 2004 .
[37] G. Folkers,et al. Synthesis and biological evaluation of 5-substituted derivatives of the potent antiherpes agent (north)-methanocarbathymine. , 2003, Journal of medicinal chemistry.
[38] E. De Clercq,et al. A thymidine phosphorylase-stable analogue of BVDU with significant antiviral activity. , 2002, Journal of medicinal chemistry.
[39] K. Erickson,et al. Ma'iliohydrin, a cytotoxic chamigrene dibromohydrin from a Philippine Laurencia species. , 2001, Journal of natural products.
[40] K. Tanaka,et al. Solvent-free organic synthesis. , 2000, Chemical reviews.
[41] J. Metzger. Solvent-Free Organic Syntheses. , 1998, Angewandte Chemie.
[42] E. De Clercq,et al. Synthesis and antiviral activity of the enantiomeric forms of carba-5-iodo-2'-deoxyuridine and carba-(E)-5-(2-bromovinyl)-2'-deoxyuridine. , 1989, Journal of medicinal chemistry.
[43] P. Ravenscroft,et al. Synthesis and antiviral properties of 5-(2-substituted vinyl)-6-aza-2'-deoxyuridines. , 1986, Journal of medicinal chemistry.
[44] E. De Clercq,et al. Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)-2'-deoxyuridines and (E)-5-(2-halovinyl)-2'-deoxycytidines. , 1985, Journal of medicinal chemistry.
[45] R. T. Walker,et al. Synthesis and antiviral properties of some 2'-deoxy-5-(fluoroalkenyl)uridines. , 1982, Journal of medicinal chemistry.