Diels–Alder reaction of quinones generated in situ by electrochemical oxidation in lithium perchlorate–nitromethane
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002485
Reference7 articles.
1. Dramatic rate accelerations of Diels-Alder reactions in 5 M lithium perchlorate-diethyl ether: the cantharidin problem reexamined
2. The lithium perchlorate-diethyl ether rate acceleration of the Diels-Alder reaction: Lewis acid catalysis by lithium ion
3. LiClO4 in Ether—an Unusual Solvent
4. LiBF4: A mild lewis acid for intramolecular diels-alder reactions.
5. Lithium perchlorate catalysis of the hetero Diels-Alder reaction: a specific lithium cation effect.
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