References
- J. B. Jones, Tetrahedron, 42, 3351 (1986).
- S. Iriuchijima and N. Kojima, Agric. Biol. Chem., 46, 1153 (1982); G. Kirchner, M. P. Scollar and A. M. Klibanov, J. Am. Chem. Soc., 107, 7072 (1985); G. Langrand, M. Secchi, G. Buono, J. Baratti and C. Triantaphylides, Tetrahedron Lett., 26, 1857 (1985); H. Kutsuki, I. Sawa, J. Hasegawa and K. Watanabe, Agric. Biol. Chem., 50, 2369 (1986); D. Breitgoff, K. Laumen and M. P. Schneider, J. Chem. Soc., Chem. Commun., 1986, 1523; J. T. Lin, T. Yamazaki and T. Kitazume, J. Org. Chem., 52, 3211 (1987); H. Hemmerle and H-J. Gais, Tetrahedron Lett., 28, 3471 (1987); P. E. Sonnet, J. Org. Chem., 52, 3477 (1987); E. Guibé-Jampel, G. Rousseau and J. Salaün, J. Chem. Soc., Chem. Commun., 1987, 1080.
- P. Cesti, A. Zaks and A. M. Klibanov, J. Solid-Phase Biochemistry, 11, 401 (1985).
- K. Yamamoto, T. Nishioka, J. Oda and Y. Yamamoto, Tetrahedron Lett., 29, 1717 (1988).
- (a) A. G. Davies and R. Feld, J. Chem. Soc., 1956, 665. (b) H. R. Williams and H. S. Mosher, J. Am. Chem. Soc., 76, 3495 (1954). (c) Y. Tatsuno and S. Otsuka, J. Am. Chem. Soc., 103, 5832 (1981).
- The lipase was kindly provided by Amano Pharmaceutical Co., Ltd.
- M. D-Castaing, B. De Jeso, S. Drouillard and B. Maillard, Tetrahedron Lett., 28, 953 (1987).
- E. Hedaya and S. Winstein, Tetrahedron Lett., 1962, 563.
- D. Battil-Robert and D. Gagnaire, Bull. Soc. Chim. Fr., 1965, 208.
- With regard to most of the racemic alcohols as substrates of lipases reported so far, the asymmetric carbon and reaction site oxygen are next to each other.
- T. A. Collyer and J. Kenyon, J. Chem. Soc., 1940, 676; H. Kwart and D. P. Hoster, J. Org. Chem., 32, 1896 (1967).
- R. H. Pickad and J. Kenyon, J. Chem. Soc., 103, 1923 (1913).