+++ Спасибо!! Tetrahedron Letters,J. Am. Chem. Soc.

[Ollax]

Здравствуйте, коллеги! Помогите найти статьи:

1. J. Org. Chem., 1997, 62 (6), pp 1568–1569
Palladium-Catalyzed Amination of Aryl Bromides: Use of Phosphinoether Ligands for the Efficient Coupling of Acyclic Secondary Amines
Jean-François Marcoux,† Seble Wagaw,‡ and Stephen L. Buchwald

DOI:

http://dx.doi.org/10.1021/jo9622946

2. J. Org. Chem., 1972, 37 (17), pp 2643–2647
Synthesis and solvolysis of 1-phenylethyl disubstituted phosphinates
Donald S. Noyce, Joseph A. Virgilio
10.1021/jo00982a001

DOI:

http://dx.doi.org/

3. Tetrahedron Letters, Volume 38, Issue 36, 8 September 1997, Pages 6363-6366
An Improved Method for the Palladium-Catalyzed Amination of Aryl Triflates
Jens Åhman and Stephen L. Buchwald

DOI:

http://dx.doi.org/10.1016/S0040-4039(97)01464-0

4. Tetrahedron Letters, Volume 39, Issue 30, 23 July 1998, Pages 5327-5330
A highly active palladium catalyst system for the arylation of anilines
Joseph P. Sadighi, Michele C. Harris and Stephen L. Buchwald

DOI:

http://dx.doi.org/10.1016/S0040-4039(98)00988-5

5.Tetrahedron Letters, Volume 39, Issue 30, 23 July 1998, Pages 5359-5362
New efficient nickel(0) catalysed amination of aryl chlorides
Eric Brenner and Yves Fort

DOI:

http://dx.doi.org/10.1016/S0040-4039(98)01105-8

6. J. Am. Chem. Soc., 1998, 120 (29), pp 7369–7370
Sterically Hindered Chelating Alkyl Phosphines Provide Large Rate Accelerations in Palladium-Catalyzed Amination of Aryl Iodides, Bromides, and Chlorides, and the First Amination of Aryl Tosylates
Blake C. Hamann and John F. Hartwig

DOI:

http://dx.doi.org/10.1021/ja981318i

Заранее благодарна за помощь!

[nikolay_ap]

3 - 5

3.pdf

4.pdf

5.pdf

[lysva]

нате)

[Ollax]

Огромное спасибо за помощь!!!!!