Affiliation:
1. Department of Chemistry Organic Chemistry School of Engineering Sciences in Chemistry Biotechnology and Health KTH Royal Institute of Technology 100 44 Stockholm Sweden
2. Centre for Analysis and Synthesis Department of Chemistry Lund University P.O. Box 24 221 00 Lund Sweden
3. Department of Theoretical Chemistry and Biotechnology School of Engineering Sciences in Chemistry Biotechnology and Health KTH Royal Institute of Technology SE 106 91 Stockholm Sweden
Abstract
AbstractAn analysis of an out‐of‐equilibrium cyclic reaction network which continuously converts a minor undesired product enantiomer to the desired major enantiomer by irreversible addition of chemical fuel and irreversible elimination of spent fuel is presented. The reaction network is maintained as long as fuel is added; interrupted fuel addition drives the system towards equilibrium, but the cyclic process restarts upon resumed fuel addition, as demonstrated by three consecutive fuel cycles. The process is powered by the hydrolysis of methyl cyanoformate to HCN and monomethyl carbonic acid, which decomposes to CO2 and MeOH. The time it takes to reach steady state depends on the rate of conversion of the fuel and decreases with increased conversion rate. Three catalysts, one metal catalyst and two enzymes, together constitute an efficient regulation system allowing control of the forward, backward and waste‐forming steps, thereby assuring the production of high yields of products with high enantiopurity.
Funder
Vetenskapsrådet
Kungliga Tekniska Högskolan
Subject
General Earth and Planetary Sciences,General Environmental Science
Cited by
1 articles.
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