Enzyme-catalyzed ring-opening polymerization of 3(S)-isopropylmorpholine-2,5-dione

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Abstract

The enzymatic ring-opening polymerization of a 6-membered cyclic depsipeptide, 3(5)-isopropylmorpholine-2,5-dione in the bulk, was investigated by using lipases as catalysts at 100 and 130°C. Unchanged monomer was recovered in the absence of the enzyme or using an inactivated enzyme, indicating that the present polymerization proceeds through enzymatic catalysis. Poly(3-isopropylmorpholine-2,5-dione) has a carboxylic acid group at one end and a hydroxy group at the other end. © Wiley-VCH Verlag GmbH, 1999.

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APA

Feng, Y., Knüfermann, J., Klee, D., & Höcker, H. (1999). Enzyme-catalyzed ring-opening polymerization of 3(S)-isopropylmorpholine-2,5-dione. Macromolecular Rapid Communications, 20(2), 88–90. https://doi.org/10.1002/(SICI)1521-3927(19990201)20:2<88::AID-MARC88>3.0.CO;2-B

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