-
Cyclophanes are well-studied
examples of
strained organic compounds.
Paracyclophanes adopt the boat
conformation normally observed in cyclohexanes. Smaller...
- [2.2]
Paracyclophane is a
cyclophane that is
applied in bio- and
materials science. It was
first synthesized by
Brown and ****hing in 1949 by pyrolyzing...
- Carbide. He
deposited parylene films by the
thermal decomposition of [2.2]
paracyclophane at
temperatures exceeding 550 °C and in
vacuum below 1 Torr. This process...
-
diastereomeren 12,15-Bis(dimethylamino) - [2](2,5) - p -benzochi****[2]
paracyclophane".
Angewandte Chemie. 90 (5): 385–386. Bibcode:1978AngCh..90..385R. doi:10...
- that has a
triplet ground-state. H. E. Winberg, F. S.
Fawcett "[2.2]
Paracyclophane"
Organic Syntheses, Coll. Vol. 5, p.883 (1973); Vol. 42, p.83 (1962)...
- Hinrichs;
Henning Hopf (2004). "Cyclophanes. Part LII:1 Ethynyl[2.2]
paracyclophanes – New
Building Blocks for
Molecular Scaffolding". Synthesis. 2004 (16):...
-
phenothiazine in toluene, it
undergoes Hofmann elimination to form [2.2]
Paracyclophane.
Paracycloheterophanes can be
obtained by
heating it with
other quaternary...
-
Phanephos can be
prepared in two
steps from [2.2]
paracyclophane. In the
first step, [2.2]
paracyclophane is
dibrominated to give a pseudo-para dibromide...
- (1990). "Diels-Alder
Reaction of 1,2,4,5-Hexatetraene: Tetramethyl[2.2]
paracyclophane-4,5,12,13-tetracarboxylate".
Organic Syntheses. 60: 41{{cite journal}}:...
-
within a
given molecules across which the
molecule is dissymmetric.
Paracyclophanes often contain chiral planes if the
bridge across the
phenylene unit...
