Intramolecular Insertion of Alkenes into Pd−N Bonds. Effects of Substrate and Ligand Structure on the Reactivity of (P−P)Pd(Ar)[N(Ar1)(CH2)3CR═CHR′] Complexes-Reference-Cited by-同舟云学术

Intramolecular Insertion of Alkenes into Pd−N Bonds. Effects of Substrate and Ligand Structure on the Reactivity of (P−P)Pd(Ar)[N(Ar1)(CH2)3CR═CHR′] Complexes

Published:2011-02-03 Issue:5 Volume:30 Page:1269-1277
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Neukom Joshua D.¹,Perch Nicholas S.¹,Wolfe John P.¹

Affiliation:

1. Department of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om200008t

Reference47 articles.

1. Selective Synthesis of 5- or 6-Aryl Octahydrocyclopenta[b]pyrroles from a Common Precursor through Control of Competing Pathways in a Pd-Catalyzed Reaction

2. Mild Conditions for Pd-Catalyzed Carboamination of N-Protected Hex-4-enylamines and 1-, 3-, and 4-Substituted Pent-4-enylamines. Scope, Limitations, and Mechanism of Pyrrolidine Formation

3. Palladium-Catalyzed Synthesis ofN-Aryl Pyrrolidines fromγ-(N-Arylamino) Alkenes: Evidence for Chemoselective Alkene Insertion into PdN Bonds

4. Oxidative Diamination of Alkenes with Ureas as Nitrogen Sources: Mechanistic Pathways in the Presence of a High Oxidation State Palladium Catalyst

5. A Facile Pd(0)-Catalyzed Regio- and Stereoselective Diamination of Conjugated Dienes and Trienes

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