References
- Akai, S., Naka, T., Fujita, T., Takebe, Y. and Kita, Y. (2000) 1-Ethoxyvinyl 2-fuorate, an efficient acyl donor for the lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted propane-1,3-diols and meso-1,2-diols, Chem. Commun. 1461–1462.
- Alexandre, F.-R. and Heut, F (1998) “Asymmetrization of meso-1,3-diols utilising Pseudomonas fluuorescens lipase”, Tetrahedron: Asymmetry 9, 2301–2310.
- Atsuumi, S., Nakano, M., Koike, Y, Tanaka, S., Ohkubo, M., Yonezawa, T., Funabashi, K., Hashimoto, J. and Morishima, H. (1990) “An efficient enantioselective preparation of 2-substituted-3-hydroxypropionic acids via chemo-enzymatic reaction”, Tetrahedron Lett. 31, 1601–1604.
- Ducret, A., Trani, M., Demers, C. and Lortie, R. (2000) “Enzymatic asymmetrization of prochiral 2-benzyl-1,3-propanediol through esterification in solvent media”, Biotechnology Lett. 22, 709–713.
- Egri, G., Balint, J., Peredi, R., Fogassy, E., Novak, L. and Poppe, L. (2000) “Lipase-catalyzed enantiotope selective acetylation of 2-acyloxypropane-1,3-diols. Influence of the acyl moiety on the selectivity”, J. Mol. Catal. B: Enzym. 10, 583–596.
- Egri, G., Fogassy, E., Novak, L. and Poppe, L. (1997) “Synthesis and lipase-catalyzed asymmetric acetylation of 3-hydroxy-2-hydroxymethylpropanal acetals”, Tetrahedron: Asymmetry 8, 547–557.
- Faber, K. (1997) Biotransformations in Organic Chemistry (Springer, Berlin).
- Faber, K., and Riva, S. (1992) Enzyme-catalyzed irreversible acyl transfer, Synthesis, 895–910.
- Guanti, G., Banfi, L. and Riva, R. (1994) “Enzymatic asymmetrization of some prochiral and meso diols through monoacetyla-tion with pig pancreatic lipase (PPL)”, Tetrahedron: Asymmetry 5, 9–12.
- Kita, Y, Naka, T., Imanishi, M., Akai, S., Takebe, Y and Matsugi, M. (1998) Asymmetric Diels-Alder reaction via enzymatic kinetic resolution using ethoxyvinyl methyl fumarate, Chem. Commun. 1183–1184.
- Kita, Y, Takebe, Y, Murata, K., Naka, T. and Akai, S. (2000) “Convenient enzymatic resolution of alcohols using highly reactive, nonharmful acyl donors, 1-ethoxyvinyl esters”, J. Org. Chem. 65, 83–88.
- Lapic, J. and Rapic, V. (2000) “Ferrocene compounds XXVIII. Synthesis of 2-(ferrocenylalkyl)- and 2[ferrocenyl(pheny-l)alkyl]-1,3-propanediols and their acetates”, Croat. Chem. Acta 73, 755–771.
- Ljubovic, E. and .S?unjic, V. (1997) “Correlation between distance of the perturbing groups and enantioselectivity of the lipase catalyzed acetylation of acyclic sec alcohols”, Tetrahedron: Asymmetry 8, 1–4.
- Poppe, L. and Novak, L. (1992) Stereoselective Biocatalysis (VCH, Weinheim, Germany), p 134.
- Santaniello, E., Ferraboschi, P. and Grisenti, P. (1990) “An efficient chemo-enzymatic approach to the enantioselective synthesis of 2-methyl-1,3-propanediol derivatives”, Tetrahedron Lett. 31, 5657–5660.
- Sehnert, J., Hess, A. and Metzler-Nolte, N. (2001) “Solution phase peptide synthesis with ferrocenyl amino acid derivatives”, J. Organomet. Chem. 637–639, 349–355.
- Shishido, K. and Bando, T. (1998) “Lipase-mediated asymmetric acetylation of prochiral diols directed towards total syntheses of biologically active molecules”, J. Mol. Catal. B: Enzym. 5, 183–186.
- Tsuji, K., Terao, Y and Achiwa, K. (1989) “Lipase-catalyzed asymmetric synthesis of chiral 1,3-propanediols and its application to the preparation of optically pure building block for renin inhibitors”, Tetrahedron Lett. 30, 6189–6192.
- van Staveren, D.R., and Metzler-Nolte, N. (2001) Labelling of [Leu(5)]-enkephalin with organometallic Mo complexes by solid-phase synthesis, Chem. Commun. 1406–1407.