Electronic Properties of Furyl Substituents at Phosphorus and Their Influence on 31P NMR Chemical Shifts-Reference-Cited by-同舟云学术

Electronic Properties of Furyl Substituents at Phosphorus and Their Influence on 31P NMR Chemical Shifts

Published:2006-06-10 Issue:26 Volume:128 Page:8434-8440
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ackermann Marco¹,Pascariu Aurelia¹,Höcher Thomas¹,Siehl Hans-Ullrich¹,Berger Stefan¹

Affiliation:

1. Contribution from the Institut für Analytische Chemie, Fakultät für Chemie und Mineralogie, Universität Leipzig, Linnéstr. 3, D-04103 Leipzig, Germany and Abteilung für Organische Chemie I, Fakultät für Naturwissenschaften, Universität Ulm, D-89069 Ulm, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja057085u

Reference56 articles.

1. 2-Furyl Phosphines as Ligands for Transition-Metal-Mediated Organic Synthesis

2. Palladium-catalyzed coupling between cephalosporin derivatives and unsaturated stannanes: A new ligand for palladium chemistry

3. Preparation of polyfunctional aryl and alkenyl zinc halides from functionalized unsaturated organolithiums and their reactivity in cross-coupling and conjugated addition reactions

4. Coordination chemistry and mechanisms of metal-catalyzed CC-coupling reactions11For Part 6 of this series, see ref. [22] (a).. Part 7. Heck vinylation of aryl halides with n-butyl acrylate: relevance of PC bond cleavage to catalyst deactivation

5. Investigations into ambient temperature biaryl coupling reactions

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