Semisynthesis of Taxol: A Highly Enantio- and Diastereoselective Synthesis of the Side Chain and a New Method for Ester Formation at C13 Using Thioesters

Angewandte Chemie (International Edition in English)

Volumn 35, Issue 15, 1996, Pages 1723-1725

  Gennari, Cesare ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0029742395     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199617231     Document Type: Article

References (6)

1. Taxol is the registered trademark of Bristol-Myers Squibb Company for Pacli-taxel. Fora review, see: K. C. Nicolaou, W.-M. Dai, R. K. Guy, Angew. Chem. 1994, 106, 38-67; Angew. Chem. Int. Ed. Engl. 1994, 33, 15-44.
2. Taxol is the registered trademark of Bristol-Myers Squibb Company for Pacli-taxel. Fora review, see: K. C. Nicolaou, W.-M. Dai, R. K. Guy, Angew. Chem. 1994, 106, 38-67; Angew. Chem. Int. Ed. Engl. 1994, 33, 15-44.
3. a) J.-N. Denis, A. E. Greene, D. Guenard, F. Gueritte-Voegelein, L. Mangatal, P. Potier, J. Am. Chem. Soc. 1988, 110, 5917-5919;
4. b) A. Commercon, D. Bezard, F. Bernard, J. D. Bouzard, Tetrahedron Lett. 1992, 33, 5185-5188;
5. c) J. N. Denis, A. M. Kanazawa, A. E. Greene, ibid. 1994, 35, 105-108; (Rhône-Poulenc Rorer S.A.), WO 94/10169, 1994, FR-A 92/13000, 1992;
6. d) A. M. Kanazawa, J. N. Denis, A. E. Greene, J. Chem. Soc. Chem. Commun. 1994, 2591-2592.