+++pyridines от Org.Chem.

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1. Functionalized 2,2‘-Bipyridines and 2,2‘:6‘,2‘ ‘-Terpyridines via Stille-Type Cross-Coupling Procedures.
Marcel Heller and Ulrich S. Schubert*
J. Org. Chem., 2002, 67 (23), pp 8269–8272

Код: Выделить всё

http://dx.doi.org/10.1021/jo0260600

2. Synthesis of 4'-vinyl-2,2':6',2''-terpyridine.
Kevin T. Potts, Dilip Konwar
J. Org. Chem., 1991, 56 (15), pp 4815–4816

Код: Выделить всё

http://dx.doi.org/10.1021/jo00015a050

3. Chemistry of heterocyclic compounds. Part 119. Synthesis of halogenated terpyridines and incorporation of the terpyridine nucleus into a polyetheral macrocycle.
George R. Newkome, David C. Hager, Garry E. Kiefer.
J. Org. Chem., 1986, 51 (6), pp 850–853

Код: Выделить всё

http://dx.doi.org/10.1021/jo00356a019

4. Construction of Preorganized Polytopic Ligands via Palladium-Promoted Cross-Coupling Reactions.
Vincent Grosshenny, Francisco M. Romero, and Raymond Ziessel.
J. Org. Chem., 1997, 62 (5), pp 1491–1500.

Код: Выделить всё

http://dx.doi.org/10.1021/jo962068w

5. Further Preparation of Substituted 2,6-Bis(2'-pyridyl)pyridines.
FRANCIS H. CASE, WALTER A. BUTTE
J. Org. Chem., 1961, 26 (11), pp 4415–4418.

Код: Выделить всё

http://dx.doi.org/10.1021/jo01069a057

Большое спосибо!

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