Stereoselective esterification of 2,6-dimethyl-1,7-heptanedioic acid, catalysed by Candida rugosa lipase

Author:

Hedenström Erik,Edlund Helen,Lund Susan

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference20 articles.

1. For an extensive review on the use of lipases in organic chemistry see: R.J. Kazlauskas, U.T. Bornscheuer, in: H.-J. Rehm, G. Reed (Eds.), Biotransformatons with Lipases. Biotechnology: Biotransformations I, vol. 8a, VCH 1998, pp. 38–191, and references cited therein.

2. See for example: N.W.J.T. Heinsman, M.C.R. Franssen, A. van der Padt, R.M. Boom, K. van’t Riet, AE. de Groot, Biocatalysis and Biotransformation 20 (2002) 297, and references cited therein.

3. Sex pheromone of pine sawflies: Enantioselective lipase catalysed transesterification of erythro-3,7-dimethylpentadecan-2-ol, diprionol

4. Sex Pheromone of the Pine Sawfly, Macrodiprion nemoralis. Stereoselective Synthesis of the Sixteen Stereoisomers of 3,7,9-Trimethyl-2-tridecyl Acetate.

5. (c) M. Larsson, B.-V. Nguyen, E. Hedenström, H.-E. Högberg, Eur. J. Org. Chem. (2001) 353.

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