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https://doi.org/10.1002/chin.199132081
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Cite Journal: ChemInform |  Publication Date: Aug 22, 2010 |
Affiliation: University of Reims Champagne-Ardenne
Abstract Enantiosalectivities up to 91% have been reached during the photodeconjugation of α, β -unsaturated esters or lactones using catalytic amounts of new chiral cyclic inductors derived from (+) camphor. Modification of the substitution on the nitrogen of the inductor can reverse the configuration of the new chiral center.
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