Preparation and Stille cross-coupling reaction of the first organotin reagents of azulenes. An efficient Pd(0)-catalyzed synthesis of 6-aryl- and biazulenes-Reference-Cited by-同舟云学术

Preparation and Stille cross-coupling reaction of the first organotin reagents of azulenes. An efficient Pd(0)-catalyzed synthesis of 6-aryl- and biazulenes

Published:2002-02 Issue:7 Volume:43 Page:1261-1264
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Okujima Tetsuo,Ito Shunji,Morita Noboru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Stille cross-coupling reaction, see e.g.: (a) Farina, V.; Krishnamurthy, V.; Scott, W. J. Org. React. 1997, 50, 1–652;

2. (b) Stille, J. K. Angew. Chem., Int. Ed. Engl. 1986, 25, 508–524.

3. Palladium-Catalyzed Vinylation of Haloazulenes and Halotropolones with Olefins. Utility of the Heck Reaction in the Conjugated Carbon Chain Preparation

4. First intermolecular palladium catalyzed arylation of an unfunctionalized aromatic hydrocarbon

5. Neuartige 2,6‐disubstituierte Azulene

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