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Chemoenzymatic synthesis of deoxy analogues of the DNA topoisomerase II inhibitor eleutherin and the 3C-protease inhibitor thysanone
Authors:Prabhakar Bachu
Affiliation:Department of Chemistry, The University of Auckland, 23 Symonds Street, Auckland, New Zealand
Abstract:The asymmetric synthesis of (−)-9-demethoxyeleutherin 6, (+)-9-demethoxyeleutherin 7 and (+)-7,9-deoxythysanone 8 has been achieved using a microwave assisted kinetic resolution of racemic alcohol 11 with Novozyme 435® as the key step.
Keywords:Eleutherin   Thysanone   Topoisomerase II inhibitor   3C-protease inhibitor   Novozyme 435®   (Candida antarctica lipase)   Microwave assisted lipase kinetic resolution   Intramolecular cyclization
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