+++J. Org. Chem.

[Marin]

Помогите, пожалуйста, со статьями:

1. Preparation of 5-Brominated and 5,5‘-Dibrominated 2,2‘-Bipyridines and 2,2‘-Bipyrimidines.
Peter F. H. Schwab, Frank Fleischer, and Josef Michl.
J. Org. Chem., 2002, 67 (2), pp 443–449

Код: Выделить всё

http://dx.doi.org/10.1021/jo010707j

2. Convenient and Efficient Synthesis of Functionalized Oligopyridine Ligands Bearing Accessory Pyrromethene-BF2 Fluorophores
Gilles Ulrich and Raymond Ziessel*
J. Org. Chem., 2004, 69 (6), pp 2070–2083

Код: Выделить всё

http://dx.doi.org/10.1021/jo035825g

3. A Versatile Strategy for the Synthesis of Functionalized 2,2‘-Bi- and 2,2‘:6‘,2‘ ‘-Terpyridines via Their 1,2,4-Triazine Analogues†
Valery N. Kozhevnikov,*‡ Dmitry N. Kozhevnikov,*§ Tatiana V. Nikitina,§ Vladimir L. Rusinov,§ Oleg N. Chupakhin,§ Manfred Zabel, and Burkhard König*‡;
J. Org. Chem., 2003, 68 (7), pp 2882–2888

Код: Выделить всё

http://dx.doi.org/10.1021/jo0267955

4. Synthesis of an All-in-One Molecule (for Organic Solar Cells)
Ole Hagemann, Mikkel Jørgensen,* and Frederik C. Krebs
J. Org. Chem., 2006, 71 (15), pp 5546–5559

Код: Выделить всё

http://dx.doi.org/10.1021/jo060491r

5. A Strategy for the Synthesis of Metal Bis(2,2‘:6‘,2‘ ‘-terpyridine)-Terminated Molecular Dyads Having Controlled Torsion Angles at the Central Biphenyl Linker
Andrew C. Benniston,* Anthony Harriman, Peiyi Li, Pritesh V. Patel, and Craig A. Sams
J. Org. Chem., 2006, 71 (9), pp 3481–3493

Код: Выделить всё

http://dx.doi.org/10.1021/jo0600555

6. N-Oxides of 2,2':6',2"-terpyridine
Randolph P. Thummel, Yurngdong Jahng
J. Org. Chem., 1985, 50 (19), pp 3635–3636

Код: Выделить всё

http://dx.doi.org/10.1021/jo00219a043

Спосибо!!!

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[Marin]

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