Highly diastereoselective Diels–Alder cycloadditions of 9R-(1-methoxyethyl)anthracene with p-benzoquinone
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2006/OB/B603819K
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1. Diels-Alder reaction of 4,6-dihydrothieno(3,4-c)furan-5,5-dioxide with quinones: Stereoselective synthesis of quinone-annelated 2,3-bis(methylene)-7-oxabicyclo(2.2.1)heptanes.
2. First synthesis of (+)-rengyolone and (+)- and (−)-menisdaurilide
3. Synthesis of differentially protected/functionalised acetylenic building blocks from p-benzoquinone and their use in the synthesis of new enediynesElectronic supplementary information (ESI) available: 400 MHz 1H NMR and 13C NMR spectra. See http://www.rsc.org/suppdata/ob/b3/b302323k/
4. Pd Catalyzed kinetic resolution of conduritol B. Asymmetric synthesis of (+)-cyclophellitol
5. Syntheses of Natural Products Having an Epoxyquinone Structure
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4. Regioselective Synthesis of Bicyclic and Polycyclic Systems by Cycloaddition Reactions of Alkenyl p-Benzoquinones;The Journal of Organic Chemistry;2017-12-08
5. Evaluating hydrogen bonding control in the diastereoselective Diels–Alder reactions of 9-(2-aminoethyl)-anthracene derivatives;Organic & Biomolecular Chemistry;2015
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