Isocyanide-based four-component synthesis of ferrocenyl 1,5-disubstituted tetrazoles
暂无分享,去创建一个
[1] P. Mirzaei,et al. A simple four-component synthesis of ferrocenyl amidodiesters and ferrocenyl triamides , 2011 .
[2] P. Patil,et al. Three-component strategy toward 5-membered heterocycles from isocyanide dibromides. , 2011, Organic letters.
[3] G. T. Cin,et al. Synthesis of novel ferrocenyl-containing pyrazolo[4,3-c]quinolines , 2011 .
[4] K. Maitra,et al. Synthesis and Characterization of New, Chiral P−N Ligands and Their Use in Asymmetric Allylic Alkylation , 2010 .
[5] P. Mirzaei,et al. A simple synthesis of ferrocenyl bis-amides by a Ugi four-component reaction , 2010 .
[6] A. Bazgir,et al. An efficient synthesis of ferrocenyl imidazo[1,2-a]pyridines , 2010 .
[7] R. Borisov,et al. Concise approach toward tetrazolo[1,5-a][1,4]benzodiazepines via a novel multicomponent isocyanide-based condensation. , 2010, Organic letters.
[8] L. Grimaud,et al. Beyond the Ugi reaction: less conventional interactions between isocyanides and iminium species , 2009 .
[9] A. Csámpai,et al. Synthesis, IR-, NMR-, DFT and X-ray study of ferrocenyl heterocycles from thiosemicarbazones. Part 21: Study on ferrocenes , 2007 .
[10] Metin Zora,et al. Synthesis of ferrocenyl pyrazoles by the reaction of (2-formyl-1-chlorovinyl)ferrocene with hydrazines , 2007 .
[11] M. M. Abd-Elzaher,et al. On the medicinal chemistry of ferrocene , 2007 .
[12] T. Torroba,et al. The use of the Ugi four-component condensation , 2007, Nature Protocols.
[13] A. Lough,et al. Synthesis, structural characterisation and biological activity of novel N -(ferrocenylmethyl)benzene-carboxamide derivatives , 2007 .
[14] Haibo Yu,et al. Synthesis and biological activity research of novel ferrocenyl-containing thiazole imine derivatives , 2007 .
[15] O. Ivashkevich,et al. Metal derivatives of tetrazoles , 2006 .
[16] H. Dai,et al. Synthesis and biological activities of new 1H-1,2,4-triazole derivatives containing ferrocenyl moiety , 2006 .
[17] Sébastien Gonnard,et al. A new and versatile Ugi/SNAr synthesis of fused 4,5-dihydrotetrazolo[1,5-a]quinoxalines , 2006 .
[18] Yoshinori Yamamoto,et al. Synthesis of 1-substituted tetrazoles via the acid-catalyzed [3+2] cycloaddition between isocyanides and trimethylsilyl azide , 2004 .
[19] G. Leclercq,et al. The first organometallic selective estrogen receptor modulators (SERMs) and their relevance to breast cancer. , 2004, Current medicinal chemistry.
[20] W. Hiller,et al. Synthesis of tetrazolopiperazine building blocks by a novel multi-component reaction , 2004 .
[21] J. Lewkowski,et al. α-(Ferrocenyl)-aminomethanephosphonous acids. First synthesis and preparation of their esters with cholesterol and adenosine , 2004 .
[22] G. Leclercq,et al. Synthesis, biochemical properties and molecular modelling studies of organometallic specific estrogen receptor modulators (SERMs), the ferrocifens and hydroxyferrocifens: evidence for an antiproliferative effect of hydroxyferrocifens on both hormone-dependent and hormone-independent breast cancer ce , 2003, Chemistry.
[23] P. Wilairat,et al. Antimalarial activity of ferrocenyl chalcones. , 2002, Bioorganic & medicinal chemistry letters.
[24] S. Bella. Second-order nonlinear optical properties of transition metal complexes , 2001 .
[25] Z. Chohan,et al. Synthesis, characterization, coordination and antibacterial properties of novel asymmetric 1,1′-disubstituted ferrocene-derived Schiff-base ligands and their Co(II), Cu(II) Ni(II) and Zn(II) complexes , 2001 .
[26] C. Biot,et al. In vitro and in vivo antimalarial activity of ferrochloroquine, a ferrocenyl analogue of chloroquine against chloroquine-resistant malaria parasites , 2001, Parasitology Research.
[27] Z. Chohan,et al. Synthesis, characterization and antibacterial properties of symmetric 1,1′-ferrocene derived Schiff-base ligands and their Co(II), Cu(II), Ni(II) and Zn(II) chelates , 2000 .
[28] S. Féry-Forgues,et al. Ferrocene and ferrocenyl derivatives in luminescent systems , 2000 .
[29] C. Biot,et al. Novel metallocenic compounds as antimalarial agents. Study of the position of ferrocene in chloroquine , 1999 .
[30] C. Richards,et al. Recent advances in the generation of non-racemic ferrocene derivatives and their application to asymmetric synthesis , 1998 .
[31] C. Biot,et al. In Vitro Antimalarial Activity of a New Organometallic Analog, Ferrocene-Chloroquine , 1998, Antimicrobial Agents and Chemotherapy.
[32] C. Biot,et al. Synthesis and antimalarial activity in vitro and in vivo of a new ferrocene-chloroquine analogue. , 1997, Journal of medicinal chemistry.
[33] G. Jaouen,et al. FACILE ROUTE TO FERROCIFEN, 1-4-(2-DIMETHYLAMINOETHOXY)-1-(PHENYL-2-FERROCENYL-BUT-1-ENE), FIRST ORGANOMETALLIC ANALOGUE OF TAMOXIFEN, BY THE MCMURRY REACTION , 1997 .
[34] Alan R. Katritzky,et al. Comprehensive Heterocyclic Chemistry IV , 1996 .
[35] A. Vessières,et al. Ferrocenyl hydroxytamoxifen: a prototype for a new range of oestradiol receptor site-directed cytotoxics , 1996 .
[36] S. Wittenberger. RECENT DEVELOPMENTS IN TETRAZOLE CHEMISTRY. A REVIEW , 1994 .
[37] E. Constable. Sandwiches Bring a New Element to Molecular Recognition , 1991 .
[38] Garland R. Marshall,et al. Conformational mimicry. 1. 1,5-Disubstituted tetrazole ring as a surrogate for the cis amide bond , 1988 .
[39] A. S. Chawla,et al. Medicinal chemistry of tetrazoles. , 1980, Progress in medicinal chemistry.
[40] T. J. KEALY,et al. A New Type of Organo-Iron Compound , 1951, Nature.