4,14-divinyl-(,)-[4.4]paracyclophane-1, 11-diene. An unusual product from a 1,10-Hofmann elimination
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. A vinylog of--xylylene. Synthesis of [2.6]paracyclophane
2. Cyclopolymerization of (E,E) - [6.2]paracyclophane-1,5-diene
3. A 1,10-hofmann elimination. Synthesis of a [6.6]paracyclopane tetraene
4. Macro Rings. XIX. Olefinic Paracyclophanes1
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1. Selected synthetic strategies to cyclophanes;Beilstein Journal of Organic Chemistry;2015-07-29
2. Hofmann Elimination;Comprehensive Organic Name Reactions and Reagents;2010-09-15
3. [4.n]Cyclophanes;Current Organic Chemistry;2009-03-01
4. Synthesis and Structure of (E,E)-[6.2]-(2,5)thiophenophane-,5-diene: a new monomer for cyclopolymerization.;Tetrahedron Letters;1992-05
5. ChemInform Abstract: 4,14-Divinyl-(E,E)-(4.4)paracyclophane-1,11-diene. An Unusual Product from a 1,10-Hofmann Elimination.;ChemInform;1987-04-28
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