Ambient Temperature, Ullmann-like Reductive Coupling of Aryl, Heteroaryl, and Alkenyl Halides
- 1 April 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (8) , 2312-2313
- https://doi.org/10.1021/jo9700078
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Copper-Mediated Cross-Coupling of Organostannanes with Organic Iodides at or below Room TemperatureJournal of the American Chemical Society, 1996
- The Asymmetric Ullmann Reaction. 2. The Synthesis of Enantiomerically Pure C2-Symmetric BinaphthylsThe Journal of Organic Chemistry, 1994
- Synthesis of unsymmetrical biaryls via kinetic higher order cyanocuprates: scope, limitations, and spectroscopic insightsJournal of the American Chemical Society, 1993
- Mechanisms of the Ullmann coupling reaction in adsorbed monolayersJournal of the American Chemical Society, 1993
- The ambient temperature Ullmann reaction and its application to the total synthesis of (.+-.)-steganacinJournal of the American Chemical Society, 1980
- Kinetics and mechanism of the copper(I)-induced homogeneous Ullmann coupling of o-bromonitrobenzeneJournal of the American Chemical Society, 1976
- Copper(I)-induced reductive dehalogenation, hydrolysis, or coupling of some aryl and vinyl halides at room temperatureThe Journal of Organic Chemistry, 1975
- Nickel-promoted synthesis of cyclic biphenyls. Total synthesis of alnusone dimethyl etherJournal of the American Chemical Society, 1975
- Synthesis with zerovalent nickel. Coupling of aryl halides with bis(1,5-cyclooctadiene)nickel(0)Journal of the American Chemical Society, 1971
- 56. 2,2′-BipyrrolesJournal of the Chemical Society, 1963