Tetracyanocorannulene – an Easily Accessible and Strongly Electron‐Deficient Compound.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 45, p. 6338, doi. 10.1002/ejoc.201801190
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- Article
Works matching DE "ANNULENE synthesis"
Results: 11
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Synthesis and Characterization of Dirhenadehydro[12]annulenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 25, p. 7194, doi. 10.1002/anie.201601562
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- Article
3
Redox-Switchable 20π-, 19π-, and 18π-Electron 5,10,15,20-Tetraaryl-5,15-diazaporphyrinoid Nickel(II) Complexes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 6, p. 2235, doi. 10.1002/anie.201510734
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- Article
4
Design and synthesis of the first triply twisted Möbius annulene.
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- Nature Chemistry, 2014, v. 6, n. 7, p. 608, doi. 10.1038/nchem.1955
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- Article
5
The chemistry of bowtiene (tricyclo[5.3.0.0<sup>2,6</sup>]decapentaene): a computational study.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 5, p. 378, doi. 10.1139/cjc-2014-0004
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- Article
6
Synthesis of dehydrobenzoannulenes with pyrene core.
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- Journal of Chemical Sciences, 2012, v. 124, n. 3, p. 597, doi. 10.1007/s12039-012-0263-z
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- Article
7
A Hybrid of Corannulene and Azacorannulene: Synthesis of a Highly Curved Nitrogen‐Containing Buckybowl.
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- Angewandte Chemie, 2018, v. 130, n. 31, p. 9966, doi. 10.1002/ange.201805678
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8
Do the writhe thing.
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- Nature Physics, 2014, v. 10, n. 7, p. 472, doi. 10.1038/nphys3027
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9
Frontispiece: Aromatic Fused [30] Heteroannulenes with NIR Absorption and NIR Emission: Synthesis, Characterization, and Excited-State Dynamics.
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- Chemistry - A European Journal, 2016, v. 22, n. 24, p. n/a, doi. 10.1002/chem.201682461
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10
Induced Correspondence of a Local π-Aromatic Sextet in Heteroannulenes: Synthesis and Characterization.
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- Chemistry - A European Journal, 2016, v. 22, n. 16, p. 5504, doi. 10.1002/chem.201600380
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11
Tetraalkoxyphenanthrene-Fused Dehydroannulenes: Synthesis, Self-Assembly, and Electronic, Optical, and Electrochemical Properties.
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- Chemistry - A European Journal, 2013, v. 19, n. 36, p. 12138, doi. 10.1002/chem.201301262
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- Article