Tetracyclo[5.2.0.01,6.02,7]nonane, A [2.1.1]propellane derivative as a reaction intermediate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Tetracyclo[5.1.0.01,6.02,7]octane, a [1.1.1]propellane derivative, and a new route to the parent hydrocarbon
2. [2.1.1.]Propellane. Reaction of 1,4-diiodobicyclo[2.1.1]hexane with tert-butyllithium and with potassium atoms
3. Silver(I) ion catalyzed rearrangements of strained .sigma. bonds. XX. Substituent effects on the generation, structural rearrangement, and deargentation of argento carbonium ions. Kinetic and product study of the silver(I)-catalyzed isomerization of C1-functionalized tricyclo[4.1.0.02.7] heptanes
4. Tricyclo[4.1.0.0 2,7 ]hept‐1(7)‐en als reaktive Zwischenstufe: Diels‐Alder‐Abfangreaktionen und Existenznachweis
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1. Synthesis and Applications of Bicyclo[1.1.0]butyl and Azabicyclo[1.1.0]butyl Organometallics;Chemistry – A European Journal;2023-04-14
2. Eliminations Involving Carbon-Halogen Bonds and Leading to Highly Strained Rings;PATAI'S Chemistry of Functional Groups;2009-12-15
3. Dihaloadamantanes: Ring Closure versus Rearrangement or Halogen-Displacement Reactions;European Journal of Organic Chemistry;2004-07
4. Thermal Behavior of [2.1.1]Propellane: A DFT/ab Initio Study;The Journal of Organic Chemistry;2003-04-10
5. Carbene−Bridgehead Olefin−Carbene Rearrangement: Formation of the Tetracyclo[4.3.0.02,8.04,7]nonane Skeleton by Carbene CH Insertion1;Journal of the American Chemical Society;1999-08-01
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