+++4 статьи амерхимобщ

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1. Highly Reactive, General and Long-Lived Catalysts for Palladium-Catalyzed Amination of Heteroaryl and Aryl Chlorides, Bromides, and Iodides: Scope and Structure−Activity Relationships [J. Am. Chem. Soc. 2008, 130, 6586-6596].
Shen, Q.; Ogata, T.; Hartwig, J. F.
J. Am. Chem. Soc.; 2008; 130(26); 8564

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http://dx.doi.org/10.1021/ja803423d

2. Highly Reactive, General and Long-Lived Catalysts for Palladium-Catalyzed Amination of Heteroaryl and Aryl Chlorides, Bromides, and Iodides: Scope and Structure–Activity Relationships
Shen, Q.; Ogata, T.; Hartwig, J. F.
J. Am. Chem. Soc.; 2008; 130(20); 6586-6596.

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http://dx.doi.org/10.1021/ja077074w

3. Electronic Effects on Reductive Elimination To Form Carbon-Carbon and Carbon-Heteroatom Bonds from Palladium(II) Complexes
Hartwig, J. F.
Inorg. Chem.; 2007; 46(6); 1936-1947.

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http://dx.doi.org/10.1021/ic061926w

4. Effects of Bases and Halides on the Amination of Chloroarenes Catalyzed by Pd(PtBu3)2
Shekhar, S.; Hartwig, J. F.
Organometallics; 2007; 26(2); 340-351.

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http://dx.doi.org/10.1021/om0607548

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