Diastereomeric control of photoinduced Diels–Alder reactions of 1-anthracen-9-yl-ethanol by hydrogen-bonding effects
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Highly diastereoselective photochemical Diels–Alder reactions: towards the development of a photoactivated chiral auxiliary
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5. Asymmetric Diels-Alder reactions with chiral dienes. Control of facial selectivity through hydrogen bonding
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1. Diels‐Alder reaction mechanisms of substituted chiral anthracene: A theoretical study based on the reaction force and reaction electronic flux;Journal of Computational Chemistry;2020-06-25
2. 1H and13C NMR assignments for a series of Diels-Alder adducts of anthracene and 9-substituted anthracenes;Magnetic Resonance in Chemistry;2015-05-27
3. Evaluating hydrogen bonding control in the diastereoselective Diels–Alder reactions of 9-(2-aminoethyl)-anthracene derivatives;Organic & Biomolecular Chemistry;2015
4. Diels–Alder reactions and transformations of 2-cyclopenten-1-one with a chiral anthracene template;Tetrahedron: Asymmetry;2011-09
5. Synthesis and Biological Evaluation of ABCD Ring Fragments of the Kibdelones;Angewandte Chemie International Edition;2011-02-18
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