Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes-Reference-Cited by-同舟云学术

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Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes

Published:2016-05-16 Issue:6 Volume:8 Page:610-617
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Niemeyer Zachary L.,Milo Anat,Hickey David P.,Sigman Matthew S.

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.2501.pdf

Reference53 articles.

1. Miyaura, N., Yamada, K. & Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett. 20, 3437–3440 (1979).

2. Wolfe, J. P., Wagaw, S. & Buchwald, S. L. An improved catalyst system for aromatic carbon−nitrogen bond formation: the possible involvement of bis(phosphine) palladium complexes as key intermediates. J. Am. Chem. Soc. 118, 7215–7216 (1996).

3. Driver, M. S. & Hartwig, J. F. A second-generation catalyst for aryl halide amination: mixed secondary amines from aryl halides and primary amines catalyzed by (DPPF)PdCl2. J. Am. Chem. Soc. 118, 7217–7218 (1996).

4. Knowles, W. S. & Sabacky, M. J. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex. Chem. Commun. 1445–1446 (1968).

5. Strohmeier, W. & Müller, F.-J. Klassifizierung phosphorhaltiger Liganden in Metallcarbonyl-Derivaten nach der π-Acceptorstärke. Chem. Ber. 100, 2812–2821 (1967).

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