-1997-

[95] 2-Methylcyclopentane-1,3-dione : an efficient synthon for the synthesis of (±)-α-cuparenone. J. Cossy, B. Gille, S. BouzBouz, V. Bellosta Tetrahedron Lett. 1997, 38, 4069-4070.

[94] A convenient procedure for the conversion of N-Boc protected pyrrolidinone derivatives into their corresponding enecarbamates. J. Cossy, M. Cases, D. Gomez Pardo Synthetic Commun. 1997, 27, 2769-2776.

[93] A short and efficient synthesis of zamifenacin a muscarinic M3 receptor antagonist. J. Cossy, C. Dumas, D. Gomez Pardo Bioorg. Med. Chem. Lett. 1997, 7, 1343-1344.

[92] A short enantioselective access to pumiliotoxin 251D from L-proline. J. Cossy, M. Cases,D. Gomez Pardo Bull. Soc. Chim. Fr. 1997, 134, 141-144.

[91] A thermal bicyclization. Synthesis of substituted 2,3,5,6-tetrahydro-6-oxo-1H-pyrrolizines. J. Cossy, D. Belotti Synlett 1997, 1249-1250.

[90] A very short and efficient synthesis of (+)-conocephalenol. J. Cossy, S. BouzBouz, A. Hakiki Tetrahedron Lett. 1997, 38, 8853-8854.

[89] A very short, efficient and inexpensive synthesis of the prodrug form of SC-54701A a platelet aggregation inhibitor. J. Cossy, A. Schmitt, C. Cinquin, D. Buisson, D. Belotti Bioorg. Med. Chem. Lett. 1997, 7, 1699-1700.

[88] An easy and efficient access to 2-bromo-4-methoxyaniline. J. Cossy, C. Poitevin, D. Gomez Pardo, J. L. Peglion Synthetic Commun. 1997, 27, 3525-3527.

[87] Cyclization of δ,ε-acetylenic amines and amino acids into cyclic enamines. A very efficient and simple access to polysubstituted pyrrolidines. J. Cossy, D. Belloti, V. Bellosta, C. Boggio Tetrahedron Lett. 1997, 38, 2677-2680.

[86] Intramolecular hene reactions. Stereo- and enantioselective synthesis of spirolactams through thermolysis of enaminocarboxamides. J. Cossy, A. Bouzide, M. Pfau J. Org. Chem. 1997, 62, 7106-7113.

[85] Photoselective bond cleavage of tricyclo[5.3.1.01,7]undecane derivatives. A facile entry to carbocyclic taxane [A,B] ring system. J. Cossy, S. BouzBouz Tetrahedron Lett 1997, 38, 1931-1932.

[84] Synthesis the (-)-pseudoconhydrine through ring enlargment of L-proline derivative. J. Cossy, C. Dumas, D. Gomez Pardo Synlett 1997, 905-906.

[83] Synthesis of ML-3000. an inhibitor of cyclooxygenase and 5-lipoxygenase. J. Cossy, D. Belotti J. Org. Chem. 1997, 62, 7900-7901.

[82] Synthesis of oxygenated heterocycles from cyclic allylsiloxanes using ring-closing olefin methathesis. C. Meyer, J. Cossy Tetrahedron Lett. 1997, 38, 7861-7864.

[81] Thermolysis of N-unsaturated alkyl-β-ketoamides. An easy access to spirolactams. J. Cossy, A. Bouzide Tetrahedron 1997, 53, 5775-5784.