bisporphyrin bullvalene

 
National Institutes of Health

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Topic mentions per year

2005-2016
01220052016

Papers overview

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2017
2017
Nature precisely manipulates primary monomer sequences in biopolymers. In synthetic polymer sequences, this precision has been… (More)
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2016
2016
The synthesis, structure, and properties of a new family of five ethane-bridged dimanganese(III) μ-hydroxo bisporphyrins with the… (More)
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2016
2016
Addition of 2,4,6-trinitrophenol (HTNP) to an ethene-bridged diiron(III) μ-oxo bisporphyrin (1) in CH2 Cl2 initially leads to the… (More)
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2013
2013
Bullvalene is an organic molecule that spontaneously undergoes Cope rearrangements, resulting in a reconfiguration of its carbon… (More)
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2012
2012
Two new supramolecular complexes consisting of an achiral bisporphyrin host and a chiral diamine guest are reported. One shows a… (More)
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2010
2010
A novel diiron(III) bisporphyrin bridged by a hydroxo group between two cofacial Fe centers is reported. X-ray structural… (More)
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2010
2010
We have designed and synthesized oligosubstituted bullvalenes 1 and 2 as adaptive molecules that can change their shapes in order… (More)
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2009
2009
Accessible and hindered phenanthroline-strapped Zn(II) porphyrin receptors exhibited suitable topography tailored to strongly and… (More)
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2009
2009
The synthesis of bisporphyrin bullvalene 1 enabled explorations of its supramolecular complexation with C(60), revealing a… (More)
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2005
2005
Epoxidation of bullvalene (1) with a neutralized solution of Oxone gave racemic trisepoxide rac-6 in 93 % isolated yield. Its… (More)
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