Reaction cascades based on squarate esters. 1,3-Dioxolane as a chaperone functional group for lithium ions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Direct elaboration of complex polyquinanes through twofold addition of vinyl anions to squarate esters
2. The Squarate Ester-1,3,5,7-Octatetraene-Polyquinane Cascade: Reaction Efficiency Is Intimately Linked to the Locus of Substitution within the Vinyl Anion
3. Successive electrocyclic rearrangements initiated by the addition of a lithiated cyclopropenone acetal to a squarate ester
4. Acetylide anions exert complete control over aldolization during the direct conversion of squarate esters into polyquinanes
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1. Applications of the Squarate Ester Cascade to the Expeditious Synthesis of Hypnophilin, Coriolin, and Ceratopicanol;Journal of the American Chemical Society;2002-07-12
2. Three-Component Coupling via the Squarate Ester Cascade as a Concise Route to the Bioactive Triquinane Sesquiterpene Hypnophilin;Organic Letters;2001-12-14
3. A study of substrate specificity of toluene dioxygenase in processing aromatic compounds containing benzylic and/or remote chiral centers;New Journal of Chemistry;2001
4. Theoretical study of the molecular mechanism of the domino pathways for squarate ester sequential reactions;J PHYS ORG CHEM;1999
5. Theoretical study of the molecular mechanism of the domino pathways for squarate ester sequential reactions;Journal of Physical Organic Chemistry;1999-01
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