Propellanes. VII. Bridgehead olefins via acetolysis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Conclusive evidence for and stereochemistry of protonation of compounds containing a bridgehead double bond in a seven-membered ring
2. Spontaneous generation of a bridgehead double bond in a seven-membered rings
3. Solvolysis of 10,10-dibromotricyclo[4,3,1,01,6]decane. Evidence for an intermediate bicyclo[4,3,1]dec-1(10)-ene derivative
4. Silver ion promoted solvolysis of 7,7-dibromobicyclo[4,1,0]heptane
5. Rearrangement of 11,11-dibromotricyclo[4.4.1.01,6]undecane
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1. 5-Hydroxybenzo[g]indoles formation from oxa-aza[3.3.3]propellanes;Tetrahedron;2015-10
2. Selective bond cleavage of [5.3.1]propellanes by lead tetraacetate: A facile entry into the carbocyclic frame [A,B ring] of taxol;Tetrahedron Letters;1995-05
3. Two Electron Systems;Organic Chemistry;1980
4. Propellanes 8. Some bent cyclopropyl cations—are they partially-opened?;Tetrahedron Letters;1978-01
5. ChemInform Abstract: PROPELLANES. VII. BRIDGEHEAD OLEFINS BY ACETOLYSIS;Chemischer Informationsdienst;1976-03-09
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