Alcohol Dehydrogenase?triggered Oxa?Michael Reaction for the Asymmetric Synthesis of Disubstituted Tetrahydropyrans and Tetrahydrofurans
(2019)
Journal Article
Eastman, H., Ryan, J., Maciá, B., Caprio, V., & O'Reilly, E. (2019). Alcohol Dehydrogenase‐triggered Oxa‐Michael Reaction for the Asymmetric Synthesis of Disubstituted Tetrahydropyrans and Tetrahydrofurans. ChemCatChem, 11(16), 3760-3762. https://doi.org/10.1002/cctc.201900658
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim An alcohol dehydrogenase-mediated asymmetric reduction and subsequent intramolecular oxa-Michael reaction has been developed for the preparation of tetrahydropyrans (or oxanes) and tetrahydrofurans,... Read More about Alcohol Dehydrogenase?triggered Oxa?Michael Reaction for the Asymmetric Synthesis of Disubstituted Tetrahydropyrans and Tetrahydrofurans.