Title: Alcohol Dehydrogenase‐Triggered Oxa‐Michael Reaction for the Asymmetric Synthesis of Disubstituted Tetrahydropyrans and Tetrahydrofurans

Authors (5): V. Caprio, H. Eastman, B. Maciá, E. O'Reilly, J. Ryan

Themes: Biocatalysis (2019)

DOI: 10.1002/cctc.201900658

Citations: 9

Pub type: article-journal

Publisher: Wiley

Issue: 16

License: http://onlinelibrary.wiley.com/termsAndConditions#vor

Publication date(s): 2019/08/21 (print) 2019/07/09 (online)

Pages: 3760-3762

Volume: 11 Issue: 16

Journal: ChemCatChem

Link: https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.201900658

URL: http://dx.doi.org/10.1002/cctc.201900658

Chemoenzymatic strategy: An alcohol dehydrogenase-triggered asymmetric reduction and subsequent intramolecular oxa-Michael reaction has been developed for the preparation of tetrahydropyrans (or oxan...

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cctc201900658-sup-0001-misc_information.pdf Supl. data for Alcohol Dehydrogenase‐Triggered Oxa‐Michael Reaction for ... 2019


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