Pyrido[3,4-c]Thiazoles through Combined Palladium-Catalysed Coupling of 2-Substituted-5-acetyl-4-thiazolyltriflates with Alkynes/Annulation Reactions

2-Substituted-5-acetyl-4-thiazolyltriflates give in good yields functionalised pyrido[3,4-c]thiazoles through combined palladium-catalysed coupling with 1-alkynes/6-endo-dig annulation reactions in the presence of ammonia.

[1]  P. Pace,et al.  A Convenient Synthesis of Nitrogen-Containing Heterocycles Bearing Amino Substituents from Heteroaryl Triflates , 1997 .

[2]  R. Rzasa,et al.  Total Synthesis of the Novel, Immunosuppressive Agent (−)-Pateamine A from Mycale sp. Employing a β-Lactam-Based Macrocyclization , 1998 .

[3]  O. Attanasi,et al.  2-Substituted 5-Acetyl-4-hydroxythiazoles. , 1998 .

[4]  S. Schreiber,et al.  Enantiomeric Binding Elements Interacting at the Same Site of an SH3 Protein Receptor , 1997 .

[5]  J. Mulzer,et al.  Synthesis of the C(11)–C(20) segment of the cytotoxic macrolide epothiline B , 1997 .

[6]  M. Gentile,et al.  Synthesis of 1,2,3,5-Substituted Pyrroles through Palladium-Catalyzed Reaction of Ethyl 2-Acetyl-4-Pentynoate Tosylhydrazone with Aryl Iodides , 1997 .

[7]  J. Herbert,et al.  New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: identification of ethyl 3-[N-[4-[4-[amino[(ethoxycarbonyl) imino]methyl]phenyl]-1,3-thiazol-2-yl]-N-[1-[(ethoxycarbonyl)methyl]pip erid -4-yl]amino]propionate (SR 121787) as a potent and long-acting antithrombotic agent. , 1997, Journal of medicinal chemistry.

[8]  A. Arcadi Regio and Stereoselective Synthesis of (E)-4-Arylidene/alkenylidene-3-tosyloxazolidin-2-ones through Palladium-Catalyzed Reactions of Aryl Iodides/Vinyl Triflates with Propargyl Tosylcarbamates , 1997 .

[9]  J. Yoshimura,et al.  TOTAL SYNTHESIS OF ANTIBIOTIC KARNAMICIN B1 , 1997 .

[10]  E. Rossi,et al.  SEQUENTIAL ADDITION/ELIMINATION/ANNULATION REACTIONS OF 4-PENTYNONES WITH BENZYLAMINE AND AMMONIA , 1997 .

[11]  E. Giralt,et al.  Synthesis and antitumor evaluation of new thiazolo[5,4-b]quinoline derivatives. , 1997, Journal of medicinal chemistry.

[12]  M. Massa,et al.  The total synthesis of the natural product endothelin converting enzyme (ECE) inhibitor, WS75624 B , 1997 .

[13]  D. Romo,et al.  A new route to 2-substituted Δ2-thiazolines: Stille cross-couplings of 2-bromo-Δ2-thiazolines , 1996 .

[14]  T. Bailey,et al.  Synthesis of 3-Pyridylpropenoic Acid Esters via Heck Coupling of Substituted 3-Pyridyl Triflates , 1995 .

[15]  E. Edstrom Synthesis of 4-Hydroxy-3-Substituted Indoles and Indolequinones via an 3-Acetyloxy-4-oxo-4,5,6,7-tetrahydroindole Intermediate , 1995 .

[16]  Y. Kondo,et al.  Palladium-Catalyzed Cross-Coupling Reaction of Haloazoles with Phenylsulfonylacetonitrile , 1992 .

[17]  Y. Kondo,et al.  Synthesis of condensed heteroaromatic compounds using palladium-catalyzed reaction , 1989 .

[18]  N. Miura,et al.  Condensed Heteroaromatic Ring Systems. XI. A Facile Synthesis of Isoquinoline N-Oxides , 1986 .

[19]  A. Ibbotson,et al.  Palladium catalysed synthesis of N and S heterocyclic esters , 1984 .

[20]  P. Stang,et al.  Perfluoroalkanesulfonic Esters: Methods of Preparation and Applications in Organic Chemistry , 1982 .

[21]  J. Sharp,et al.  The reactions of 2-alkynylbenzaldehydes with hydrazides: a route to isoquinoline N-imines , 1980 .

[22]  P. Stang,et al.  Single-Step Improved Synthesis of Primary and Other Vinyl Trifluoromethanesulfonates , 1980 .