Syn-5,13-dimethyl[2.2]metacyclophane. Synthesis, spectra and thermal stability
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. syn-[2.2]Metacyclophane: synthesis and facile isomerization to anti-[2.2]metacyclophane. The use of (arene)chromium carbonyl complexes to control the stereochemistry of cyclophanes
2. A fusion of metals, cyclophanes and dihydropyrenes
3. Transformation of sulfide linkages to carbon-carbon double bond. Syntheses of cis- and trans-15,16-dimethyldihydropyrene and trans-15,16-dihydropyrene
4. Syntheses of syn-[2.2]metacyclophanes and triple-layered anti-[2.2]metacyclophanes
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1. Synthesis and conformations of [2.n]metacyclophan-1-ene epoxides and their conversion to [n.1]metacyclophanes;Organic & Biomolecular Chemistry;2017
2. Dynamical Excimer Formation in Rigid Carbazolophane via Charge Transfer State;The Journal of Physical Chemistry A;2013-08-02
3. Pyrolysis of Dimethoxy[n.2]Metacyclophanes: An Intramolecular Condensation Reaction to Give Oxa[n.2.1](1,3,2)Cyclophanes;Journal of Chemical Research;2012-03
4. Synthesis of 4,16-Dimethoxy-1,2-Dimethyl[2.4]Metacyclophan-1-Ene and 8,17-Dimethoxy-1.2-Dimethyl-10-Thia[2.3.4](1,3,5)Cyclophan-1-Ene;Journal of Chemical Research;2010-08
5. Medium-size Cyclophanes, 77.1 Synthesis and addition of Bromine to syn-[2.n]meta-cyclophan-1-enes;Journal of Chemical Research;2007-11
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