Carbonylative lactonization via carbonyl oxygen attack: a short and selective total synthesis of uncinine and its analogues

[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 .