Carbonylative lactonization via carbonyl oxygen attack: a short and selective total synthesis of uncinine and its analogues
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J. Kuneš | M. Pour | Petr Šenel | H. Fáková
[1] T. Holas,et al. Biodegradable derivatives of tranexamic acid as transdermal permeation enhancers. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[2] A. Punzi,et al. New stereoselective methodology for the synthesis of dihydroxerulin and xerulin, potent inhibitors of the biosynthesis of cholesterol , 2004 .
[3] S. Katsumura,et al. Stereocontrolled total synthesis of a polyfunctional carotenoid, peridinin. , 2004, The Journal of organic chemistry.
[4] I. Císařová,et al. Neighboring group effect in Pd-catalyzed carbonylation terminated by lactonization: a need for a protective group and/or DMF. , 2004, The Journal of organic chemistry.
[5] R. Brückner,et al. Total synthesis of xerulinic acid. , 2004, Angewandte Chemie.
[6] H. Elsohly,et al. Antifungal cyclopentenediones from Piper coruscans. , 2004, Journal of the American Chemical Society.
[7] M. Yun,et al. 5-Arylidene-2(5H)-furanone derivatives: synthesis and structure-activity relationship for cytotoxicity , 2004, Archives of pharmacal research.
[8] J. Parrain,et al. Regio- and stereoselective preparation of γ-alkylidenebutenolides or α-pyrones using a Stille reaction and palladium-catalysed oxacyclisation sequence , 2003 .
[9] C. Anselmi,et al. Mucochloric Acid: A Useful Synthon for the Selective Synthesis of 4‐Aryl‐3‐chloro‐2(5H)‐furanones, (Z)‐4‐Aryl‐5‐[1‐(aryl)methylidene]‐3‐chloro‐2(5H)‐furanones and 3,4‐Diaryl‐2(5H)‐furanones , 2003 .
[10] N. Risch,et al. γ-Regioselectivity of (furan-2-yloxy)-trimethyl-silane towards iminium salts: synthesis of γ-arylidenebutenolides , 2003 .
[11] J. Sweeney,et al. Recent developments in the synthesis of furan-2(5H)-ones , 2002 .
[12] E. Negishi,et al. Catalytic and selective conversion of (Z)-2-en-4-ynoic acids to either 2H-pyran-2-ones in the presence of ZnBr2 or (Z)-5-alkylidenefuran-2(5H)-ones in the presence of Ag2CO3 , 2002 .
[13] C. Anselmi,et al. Total synthesis of rubrolide M and some of its unnatural congeners , 2002 .
[14] Maria Novella Romanelli,et al. Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs. , 2002, Current pharmaceutical design.
[15] L. Mannina,et al. Selective synthesis of (Z)-4-aryl-5-[1-(aryl)methylidene]-3-bromo-2(5H)-furanones , 2001 .
[16] F. Chang,et al. The alkaloids of Artabotrys uncinatus. , 2001, Journal of natural products.
[17] R. Bruckner. The Synthesis of gama-Alkylidenebutenolides , 2001 .
[18] R. Brueckner. The -elimination route to stereodefined ?-alkylidenebutenolides , 2001 .
[19] J. Suh,et al. Artificial Trinuclear Metallopeptidase Synthesized by Cross-Linkage of a Molecular Bowl with a Polystyrene Derivative , 2000 .
[20] L. Mannina,et al. Palladium-catalyzed synthesis of stereodefined 3-[(1,1-unsymmetrically disubstituted)methylidene]isobenzofuran-1(3H)-ones and stereodefined 5-[(1,1-unsymmetrically disubstituted)methylidene]furan-2(5H)-ones , 2000 .
[21] J. Parrain,et al. Halolactonisation of (2Z,4E)-dienoic Acids. A Novel Approach to γ-Alkylidene Butenolides , 2000 .
[22] L. Mannina,et al. A New Stereocontrolled Synthesis of Dihydroxerulin, a Potent Noncytotoxic Inhibitor of the Biosynthesis of Cholesterol , 2000 .
[23] A. Alimardanov,et al. An efficient and stereoselective synthesis of xerulin via Pd-catalyzed cross coupling and lactonization featuring (E)-lodobromoethylene as a novel two-carbon synthon. , 2000, Organic letters.
[24] J. Parrain,et al. (E)-5-(Tributylstannylmethylidene)-5H-furan-2-ones: versatile synthons for the stereospecific elaboration of gamma-alkylidenebutenolide skeletons. , 1999, Organic letters.
[25] E. Negishi,et al. A highly efficient and selective synthesis of lissoclinolide featuring hydrogen transfer hydrozirconation,trans-selective Pd-catalyzed cross coupling of alkenylzirconiums with 1,1-dibromoalkenes and Ag-catalyzed lactonization providing(Z)-γ-alkylidenebutenolides , 1999 .
[26] M. Ouellet,et al. Facile access to 4-aryl-2(5H)-furanones by Suzuki cross coupling: Efficient synthesis of rubrolides C and E , 1998 .
[27] L. Mannina,et al. STEREOCONTROLLED SYNTHESIS OF LISSOCLINOLIDE BY SEQUENTIAL TRANSITION METAL-CATALYZED LACTONIZATION/CROSS-COUPLING REACTIONS , 1998 .
[28] P. Tuchinda,et al. γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: a simple synthesis of γ-arylidenebutenolides , 1998 .
[29] L. Mannina,et al. A novel protocol for the stereoselective synthesis of variously substituted (Z)-5-ylidene-5H-furan-2-ones , 1998 .
[30] Fang Liu,et al. Efficient and Stereoselective Synthesis of Freelingyne via Pd-Catalyzed Cross Coupling and Lactonization(1). , 1997, The Journal of organic chemistry.
[31] E. Negishi,et al. Regio- and stereoselective synthesis of ?-alkylidenebutenolides and related compounds , 1997 .
[32] E. Negishi,et al. Highly Efficient and Selective Procedures for the Synthesis of γ-Alkylidenebutenolides via Palladium-Catalyzed Ene-Yne Coupling and Palladium- or Silver Catalyzed Lactonization of (Z)-2-En-4-ynoic Acids. Synthesis of Rubrolides A, C, D, and E , 1997 .
[33] C. Copéret,et al. Acylpalladation of Internal Alkynes and Palladium-Catalyzed Carbonylation of (Z)-.beta.-Iodoenones and Related Derivatives Producing .gamma.-Lactones and .gamma.-Lactams , 1995 .
[34] B. D. Harris,et al. A Reductive Amination/Lactamization Procedure Using Borohydride Reagents , 1994 .
[35] D. Knight. Synthetic approaches to butenolides , 1994 .
[36] N. Didry,et al. Microbiological properties of protoanemonin isolated from Ranunculus bulbosus , 1993 .
[37] R. Andersen,et al. Rubrolides A-H, metabolites of the colonial tunicate Ritterella rubra , 1991 .
[38] T. Anke,et al. Antibiotics from basidiomycetes. XXXVII. New inhibitors of cholesterol biosynthesis from cultures of Xerula melanotricha Dörfelt. , 1990, The Journal of antibiotics.
[39] M. Martin,et al. In vitro activity of protoanemonin, an antifungal agent. , 1990, Planta medica.
[40] S. Denmark,et al. (E)-3-(Trimethylsilyl)-2-propen-1-ol. An Improved Preparation , 1983 .
[41] E. Corey,et al. A method for selective conversion of allylic and benzylic alcohols to halides under neutral conditions , 1972 .