Addition of arylboronic acids to symmetrical and unsymmetrical azo compounds

K Kisseljova, O Tšubrik, R Sillard, S Mäeorg…

Index: Kisseljova, Ksenija; Tsubrik, Olga; Sillard, Rannar; Maeeorg, Sirje; Maeeorg, Uno Organic Letters, 2006 , vol. 8, # 1 p. 43 - 45

Full Text: HTML

Citation Number: 36

Abstract

Arylation of hydrazines, which are a special class of nitrogen compounds, is of high interest because of their pharmaceutical importance. Both organobismuth reagents 5b,8 and aryl iodides 9 were recently used in the preparation of substituted hydrazines, whereas Lan's and Lam's works involved arylboronic acids. 3,6 All these methods start with a N−H compound, although substituted hydrazines can also be obtained by addition of an aryl-containing nucleophile to azo compound. The ...

Related Articles:

4??Substituted tert??Butyl Phenylazocarboxylates—Synthetic Equivalents for the para??Phenyl Radical Cation

[Hoefling, Sarah B.; Bartuschat, Amelie L.; Heinrich, Markus R. Angewandte Chemie - International Edition, 2010 , vol. 49, # 50 p. 9769 - 9772]

Examination of Synthetic Routes to Monosubstituted Diimides. II. Synthesis of t-Butyl Aryl-and Acylazoformates. Acid-Induced Cleavage of the Thionocarbo-t-butoxy …

[Carpino,L.A. et al. Journal of Organic Chemistry, 1961 , vol. 26, p. 4336 - 4340]

More Articles...