Die stereochemie ortho-substituierter triphenylamin-derivate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Heteropolycyclen vom Triangulen‐Typ, I. 8.12‐Dihydro‐4H‐benzo[1.9]chinolizino[3.4.5.6.7‐ defg ]acridin‐trion‐(4.8.12) und 5.9‐Dihydro‐chino[3.2.1‐ de ]acridin‐dion‐(5.9)
2. Pyramidale Inversion
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2. Substituent effects on the redox properties and structure of substituted triphenylamines. An experimental and computational study;Tetrahedron;2009-03
3. Ion-Bearing Propellers: Alkali Metal Complexes of Tris(2-alkoxyphenyl)amine Ionophores;Inorganic Chemistry;1996-01-01
4. Syntheses of Azulene Analogues of Triphenylmethyl Cation: Extremely Stable Hydrocarbon Carbocations and the First Example of a One-Ring Flip as the Threshold Rotation Mechanism for Molecular Propellers;Bulletin of the Chemical Society of Japan;1995-05
5. Dynamic stereochemistry of tri(3-methyl-1-azulenyl)methyl cation; the first example of one-ring flip mechanism;Tetrahedron Letters;1992-10
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