Diastereoselective intramolecular Diels-Alder reaction of the furan diene. A facile access to enantiopure epoxy tetrahydroisoindolines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. THE ASYMMETRIC DIELS–ALDER REACTIONS OF α,β-UNSATURATED CARBOXYLIC AMIDES DERIVED FROM (−)-PHENYLGLYCINOL AND THE ASYMMETRIC TOTAL SYNTHESIS OF (+)-FARNESIFEROL C
2. Synthetic studies on the avermectins: substituent effects on intramolecular Diels-Alder reactions of N-furfurylacrylamides and further reactions of the cycloadducts
3. Asymmetric synthesis of methyl N-(1-phenylethyl)-3-aza-10-oxatricyclo[5.2.1.01,5]-4-oxo dec-8-en-6-carboxylate by an intramolecular Diels-Alder reaction
4. Thermodynamically controlled asymmetric induction: Applications with the intramolecular Diels-Alder reaction involving a furan diene
5. Multiple equilibration strategies in synthesis. Stereocontrolled synthesis of polypropionate fragments
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1. Toward Understanding CB[7]-Based Supramolecular Diels-Alder Catalysis;Frontiers in Chemistry;2020-11-06
2. Parallel Kinetic Resolution of Intramolecular Furan Diels-Alder Cycloadducts via Asymmetric Hydroboration;European Journal of Organic Chemistry;2019-11-08
3. Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions;Angewandte Chemie International Edition;2017-11-03
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