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Dehydrohalogenation of the Bis-dihalocarbene Adducts of Some Methoxycyclohexa-1,4-dienes: Revision of Product Structures

MG Banwell, RW Gable, B Halton and JR Phyland
47(10) pp.1879 - 1884


6 articles found in Crossref database.

ChemInform Abstract: Dehydrohalogenation of the Bis‐dihalocarbene Adducts of Some Methoxycyclohexa‐1,4‐dienes: Revision of Product Structures.
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Mechanistic Studies on the Base-Promoted Conversion of Alkoxy-Substituted, Ring-Fused gem-Dihalocyclopropanes into Furans: Evidence for a Process Involving Electrocyclic Ring Closure of a Carbonyl Ylide Intermediate
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Mechanistic Studies on the Base-Promoted Ring Opening of Glycal-Derived gem-Dibromocyclopropanes
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Dichlorocarbene adducts of alkyl enol ethers as precursors to furans: application to a total synthesis of the furanosesquiterpene (±)-pallescensin A
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Tetrahedron Letters. 2006 47(38). p.6817
Synthesis of Oxepines and 2-Branched Pyranosides from a d-Glucal-Derived gem-Dibromo-1,2-cyclopropanated Sugar
Hewitt Russell J., Harvey Joanne E.
The Journal of Organic Chemistry. 2010 75(3). p.955

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