Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Aryl Halides
作者:Jeongju Moon、Mihee Jang、Sunwoo Lee
DOI:10.1021/jo802290r
日期:2009.2.6
2-Octynoic acid and phenylpropiolic acid were employed for the palladium-catalyzed decarboxylative coupling reaction and with a variety of arylhalides. The former needed 1,4-bis(diphenylphosphino)butane (dppb) as a ligand and the latter tri-tert-butylphosphine (PtBu3), and both required 2 equiv of tetra-n-butylammonium fluoride (TBAF) for full conversion. These reactions showed high reactivities and
A palladium-catalyzed, iodine-mediatedelectrophilicannulation between 2-(1-alkynyl)biphenyl and disulfide has been developed. With the combination of PdCl2 and I2, a variety of 2-(1-alkynyl)biphenyls underwent electrophilicannulations with various disulfides successfully to afford the corresponding 9-sulfenyl phenanthrenes in moderate to excellent yields.
Synthesis of Fluorenes<i>via</i>the Palladium-Catalyzed 5-<i>exo-dig</i>Annulation of<i>o</i>-Alkynylbiaryls
作者:Natalia Chernyak、Vladimir Gevorgyan
DOI:10.1002/adsc.200800765
日期:2009.5
The direct Pd-catalyzed intramolecular rapidly with electron-deficient benzene ring, which, in hydroarylation of o-alkynyl biaryls proceeded in highly combination with a substantial isotope effect observed, stereoselective manner producing fluorenes 2, the products of 5-exo-dig cyclization, in excellent yields. The cascade intermolecular arylation, incorporated in this transformation, allowed for efficient
One-Pot Synthesis of Diarylalkynes Using Palladium-Catalyzed Sonogashira Reaction and Decarboxylative Coupling of sp Carbon and sp<sup>2</sup> Carbon
作者:Jeongju Moon、Miso Jeong、Hyungoog Nam、Jinhun Ju、Joong Ho Moon、Hyun Min Jung、Sunwoo Lee
DOI:10.1021/ol703130y
日期:2008.3.1
Decarboxylative coupling of sp-sp2 carbons is possible by palladium catalyst. Employing propiolic acid (1) as a difunctional alkyne, and using the consecutive reactions of the Sonogashira reaction and the decarboxylative coupling, unsymmetrically substituted diaryl alkynes were obtained in moderate to good yield.