Lipase AH-catalyzed asymmetric synthesis of (S)-(-)-NB 818

Heterocycles

Volumn 42, Issue 1, 1996, Pages 169-171

  Yamazaki, Yukiyoshi ^a   Achiwa, Kazuo ^a  

^a UNIVERSITY OF SHIZUOKA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0342686905     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-95-7139     Document Type: Article

References (14)

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3. T. Nakazawa, Y. Fukuta, Y. Tanaka, K. Ishii, and K. Nakayama, Folia Japonica, 1994, 103, 47.
4. Y. Yamazaki, H. Ebiike, and K. Achiwa, Chem. Pharm. Bull., 1994, 42, 1968.
5. Many enzymatic reactions were applied to enantioselective synthesis. Recent reviews see.: E, Santaniello, P. Ferraboschi, P. Grisenti, and A. Manzocchi, Chem. Rev., 1992, 92, 1071. M. Murata, H. Ebiike, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1991, 49, 1127. E. Mizuguti, H. Nagai, H. Uchida, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1994, 52, 638.
6. Many enzymatic reactions were applied to enantioselective synthesis. Recent reviews see.: E, Santaniello, P. Ferraboschi, P. Grisenti, and A. Manzocchi, Chem. Rev., 1992, 92, 1071. M. Murata, H. Ebiike, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1991, 49, 1127. E. Mizuguti, H. Nagai, H. Uchida, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1994, 52, 638.
7. Many enzymatic reactions were applied to enantioselective synthesis. Recent reviews see.: E, Santaniello, P. Ferraboschi, P. Grisenti, and A. Manzocchi, Chem. Rev., 1992, 92, 1071. M. Murata, H. Ebiike, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1991, 49, 1127. E. Mizuguti, H. Nagai, H. Uchida, and K. Achiwa, Journal of Synthetic Organic Chemistry, Japan, 1994, 52, 638.
8. B. Lamm, R. Simonsson, and S. Sundell, Tetrahedron Lett., 1989, 30, 6423.
9. Determined by using CHIRALPAK AS (n-hexane/ 2-propanol= 30/ 1).
10. 3).
11. H. Ebiike and K. Achiwa, Tetrahedron: Asymmetry, 1994, 5, 1447.
12. When racemic 6 was hydrolyzed, there were a few deprotected compounds. So (S)-(-)-6 was converted to (S)-(-)-7 without isolation of the intermediates.
13. 3).
14. Determined by using CHIRALPAK AS (n-hexane/ 2-propanol= 3/ 1).