(7R,8R,8aS)-8-Hydroxy-7-phenylperhydroindolizin-3-one
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Jozef Kožíšek | Viktor Vrábel | Ľubomír Švorc | Jozefína Žúžiová | Mária Bobošíková | Ľ. Švorc | J. Kožíšek | V. Vrabel | J. Žúžiová | Mária Bobošíková
[1] A. Bast,et al. Synthesis of 1-Substituted 7-Cyano-2,3-diphenylindolizines and Evaluation of Antioxidant Properties , 2000 .
[2] R. Bronson,et al. In vivo analysis of castanospermine, a candidate antiretroviral agent. , 1989, Journal of acquired immune deficiency syndromes.
[3] S P Gupta,et al. A quantitative structure-activity relationship study on a novel class of calcium-entry blockers: 1-[(4-(aminoalkoxy)phenyl)sulphonyl]indolizines. , 2003, European journal of medicinal chemistry.
[4] François Delattre,et al. 1-(4-Nitrophenoxycarbonyl)-7-pyridin-4-yl indolizine: a new versatile fluorescent building block. Application to the synthesis of a series of fluorescent β-cyclodextrins , 2005 .
[5] V. Gevorgyan,et al. Regiodivergent metal-catalyzed rearrangement of 3-iminocyclopropenes into N-fused heterocycles. , 2007, Organic letters.
[6] G. Sheldrick. A short history of SHELX. , 2008, Acta crystallographica. Section A, Foundations of crystallography.
[7] Yuanhong Liu,et al. Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and alkynes under solvent-free conditions or in water. , 2007, Organic letters.
[8] Synthesis of the new mannosidase inhibitors, diversity-oriented 5-substituted swainsonine analogues, via stereoselective Mannich reaction. , 2004, Organic letters.
[9] Mikael Bols,et al. Recent developments of transition-state analogue glycosidase inhibitors of non-natural product origin. , 2002, Chemical reviews.
[10] K. Wassermann,et al. Synthesis and pharmacology of a novel pyrrolo[2,1,5-cd] indolizine (NNC 45-0095), a high affinity non-steroidal agonist for the estrogen receptor. , 2000, Bioorganic & medicinal chemistry letters.
[11] Yuanhong Liu,et al. General and direct synthesis of 3-aminoindolizines and their analogues via Pd/Cu-catalyzed sequential cross-coupling/cycloisomerization reactions. , 2007, Organic letters.
[12] Owen Johnson,et al. CIF applications. XV. enCIFer: a program for viewing, editing and visualizing CIFs , 2004 .
[13] W. B. Harrell. Mannich bases from 1,2-diphenylindolizine: ephedrine and methamphetamine as amine components. , 1970, Journal of pharmaceutical sciences.
[14] A. Rotaru,et al. A Novel Coupling 1,3-Dipolar Cycloaddition Sequence as a Three-Component Approach to Highly Fluorescent Indolizines , 2005 .
[15] T. Butters. Control in the N-linked glycoprotein biosynthesis pathway. , 2002, Chemistry & biology.
[16] Ivone Carvalho,et al. α- and β-Glucosidase inhibitors: chemical structure and biological activity , 2006 .
[17] L. Gundersen,et al. Antimycobacterial Activity of 1‐Substituted Indolizines , 2003, Archiv der Pharmazie.
[18] L. Juillerat-Jeanneret,et al. Glycosylation pathways as drug targets for cancer: glycosidase inhibitors. , 2006, Mini reviews in medicinal chemistry.
[19] C. Brown,et al. The crystal structure of acetanilide , 1954 .
[20] Jozef Kožíšek,et al. 2,4,4a,5,6,7,9,9a-Octahydrofuro[2,3-f]indolizin-7-one , 2004 .
[21] Charles H. Stirton,et al. Castanospermine in Alexa species , 1988 .
[22] Eric Deniau,et al. First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin , 2000 .
[23] N. Prónayová,et al. Highly diastereoselective approach to novel phenylindolizidinols via benzothieno analogues of tylophorine based on reductive desulfurization of benzo[b]thiophene , 2009 .
[24] P. Compain,et al. Carbohydrate mimetics-based glycosyltransferase inhibitors. , 2001, Bioorganic & medicinal chemistry.
[25] D. Cremer,et al. General definition of ring puckering coordinates , 1975 .
[26] R. Sarpong,et al. Pt-catalyzed cyclization/1,2-migration for the synthesis of indolizines, pyrrolones, and indolizinones. , 2007, Organic letters.
[27] A. Kel'in,et al. A novel Cu-assisted cycloisomerization of alkynyl imines: efficient synthesis of pyrroles and pyrrole-containing heterocycles. , 2001, Journal of the American Chemical Society.
[28] Ying Cheng,et al. Concise and divergent total synthesis of swainsonine, 7-alkyl swainsonines, and 2,8a-diepilentiginosine via a chiral heterocyclic enaminoester intermediate , 2008 .
[29] Jozef Kožíšek,et al. (11R,11aS)-11-Hydroxy-1,5,11,11a-tetrahydro-1-benzothieno[2,3-f]indolizin-3(2H)-one , 2008, Acta crystallographica. Section E, Structure reports online.
[30] E. Stoll,et al. The Crystal and Molecular Structure of N-Methylacetanilide. , 1967 .
[31] M. Gelb,et al. Highly specific and broadly potent inhibitors of mammalian secreted phospholipases A2. , 2008, Journal of medicinal chemistry.
[32] J. S. Reid,et al. The Analytical Calculation of Absorption in Multifaceted Crystals , 1995 .
[33] J. Jaung,et al. 1,3-Dipolar Cycloaddition Reactions of Pyridinium Azomethine Ylides Containing 5,6-Dicyanopyrazines , 2003 .
[34] W. Snowden,et al. Synthesis and Anti-Herpes Activity of a Series of Indolizines , 1995 .
[35] B. Norberg,et al. 8,8′-Dichloro-1,1′,5,5′-tetrahydro-10,10′-bipyrrolo[1,2-b]isoquinoline-3,3′(2H,2′H)-dione , 2003 .
[36] L. Gundersen,et al. Indolizine 1-sulfonates as potent inhibitors of 15-lipoxygenase from soybeans. , 2005, Bioorganic & medicinal chemistry.
[37] L. James,et al. Loco intoxication: indolizidine alkaloids of spotted locoweed (Astragalus lentiginosus). , 1982, Science.