First asymmetric synthesis of (-)-(2S, 3R)-methanoproline

Tetrahedron Asymmetry

Volumn 7, Issue 5, 1996, Pages 1267-1268

  Hercouet, Alain ^a   Bessières, Bernard ^a   Le Corre, Maurice ^a  

^a UNIVERSITÉ DE RENNES 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2,3 METHANOPROLINE; PROLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0029890924     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00139-5     Document Type: Article

References (13)

1. For recent reviews see: (a), Stammer C. H., Tetrahedron, 1990, 46, 2231.
2. (b) Alami A., Calmes M., Daunis J. and Jacquier R., Bull. Soc. Chim. Fr., 1993, 130, 5.
3. (c) Burgess K., Ho K. K. and Moye-Sherman D., Synlett, 1994, 575.
4. Le Corre M., Hercouët A. and Bessières B., Tetrahedron: Asymmetry, 1995, 6, 683.
5. Hercouët A., Bessières B. and Le Corre M., Tetrahedron: Asymmetry, 1996, 7, 283.
6. Switzer F. L., Van Halbeek H., Holt E. M., Stammer C. H. and Salveit M. E., Tetrahedron, 1989, 45, 6091.
7. Matsui S., Srivastava V. P., Holt E. M., Taylor E. W. and Stammer C. H., Int. J. Peptide Protein Res., 1991, 37, 306.
8. Hanessian S., Ugolini A., Dubé D. and Glamyan A., Can. J. Chem., 1984, 62, 2146.
9. 3) δ 35.45 and 36.61; 40.25 and 40.77; 70.43 and 71.26; 77.48 and 80.42.
10. Gao Y. and Sharpless K. B., J. Am. Chem. Soc., 1988. 110, 7538.
11. Stork G., Leong A. Y. W. and Touzin A. M., J. Org. Chem., 1976, 41, 3491.
12. 3) δ 19.26, 24.19, 30.03, 38.40, 44.05, 53.38 and 169.73.
13. 2O) δ 15.57, 27.28, 27.31, 45.40, 51.16 and 176.81.