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Synfacts 2011(10): 1130-1130
DOI: 10.1055/s-0030-1261121
DOI: 10.1055/s-0030-1261121
Organo- and Biocatalysis
© Georg Thieme Verlag
Stuttgart ˙ New York
Asymmetric Olefin Isomerization of Butenolides
Y. Wu, R. P. Singh, L. Deng*
Brandeis University, Waltham, USA
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
20. September 2011 (online)

Significance
Deng and co-workers describe an asymmetric olefin isomerization of butenolides via proton-transfer catalysis using catalysts 1 and 2. The authors developed new cinchona-derived catalysts 1 and 2, and these catalysts gave the products in high enantioselectivities and good yields. A proposed mechanism was shown, and this catalytic cycle is comparable to the enzyme-mediated isomerization of steroidal ketones. To prove the reaction mechanism, the authors carried out preliminary kinetic studies and kinetic-isotope-effect experiments and the protonation step turned out to be the rate-determining step.