This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
K. Faber, S. F. Mayer, W. Kroutil, Enzyme-Initiated Domino-(Cascade)-Reaction, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01912
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Enzyme-Initiated Domino-(Cascade)-Reaction
W. Kroutil 1
S. F. Mayer 1
K. Faber 1
1. Department of Chemistry, Organic & Bioorganic Chemistry, University of Graz, Heinrichstrasse 28, A-8010 Graz, Austria
Abstract
An impressive number of chemo-catalyzed cascade-reactions (especially those involving cyclizations) have been accomplished by using palladium [1-3]. Other types of typical cascade-reactions (although they have been denoted as 'tandem-reactions' in the respective publications) have been reviewed and classified according to their type of mechanism [4]. All of these reaction sequences were initiated by an organic or inorganic catalyst, or by thermal reactions. On the contrary, only few examples of cascade-reactions have been reported, where the initiation of the reaction cascade consisted of a biotransformation [5]. Taking advantage of the unparalleled diastereo- and enantio-specificity of enzymes, in many cases the reaction cascade was turned into an asymmetric fashion which furnished non-racemic product(s).
Keywords
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