Dynamic kinetic resolution of transient hemiketals: a strategy for the desymmetrisation of prochiral oxetanols
Author:
Affiliation:
1. Organisch-Chemisches Institut, Westfälische Wilhelms-Universität, Corrensstraße 36, 48149 Münster, Germany
2. Department Chemie, Johannes Gutenberg-Universität, Duesbergweg 10-14, 55128 Mainz, Germany
Abstract
Funder
Verband der Chemischen Industrie
Studienstiftung des Deutschen Volkes
Westfälische Wilhelms-Universität Münster
Johannes Gutenberg-Universität Mainz
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC01547A
Reference53 articles.
1. Diastereoselective synthesis of protected syn 1,3-diols by base-catalyzed intramolecular conjugate addition of hemiacetal-derived alkoxide nucleophiles
2. Diastereoselective Construction of syn-1,3-Dioxanes via a Bismuth-Mediated Two-Component Hemiacetal/Oxa-Conjugate Addition Reaction
3. Diastereoselective construction of anti-4,5-disubstituted-1,3-dioxolanes via a bismuth-mediated two-component hemiacetal oxa-conjugate addition of γ-hydroxy-α,β-unsaturated ketones with paraformaldehyde
4. Stereoselective Tandem Synthesis of syn-1,3-Diol Derivatives by Integrating Olefin Cross-Metathesis, Hemiacetalization, and Intramolecular Oxa-Michael Addition
5. Novel asymmetric oxy-michael addition reaction of the chiral ketones to the achiral ?- or ?-hydroxy-?,?-unsaturated carbonyl compounds
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1. Ring opening of photogenerated azetidinols as a strategy for the synthesis of aminodioxolanes;Beilstein Journal of Organic Chemistry;2024-07-19
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