Stereochemical Outcome of Copper-Catalyzed C–H Insertion Reactions. An Experimental and Theoretical Study-Reference-Cited by-同舟云学术

Stereochemical Outcome of Copper-Catalyzed C–H Insertion Reactions. An Experimental and Theoretical Study

Published:2013-06-05 Issue:12 Volume:78 Page:5851-5857
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jiménez-Osés Gonzalo¹,Vispe Eugenio²,Roldán Marta²,Rodríguez-Rodríguez Sergio²,López-Ram-de-Viu Pilar²,Salvatella Luis²,Mayoral José A.²,Fraile José M.²

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, California 90095-1569, United States

2. Instituto de Síntesis Química y Catálisis Homogénea, Facultad de Ciencias, Universidad de Zaragoza-CSIC, 50009 Zaragoza, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400415b

Reference69 articles.

1. The Assignment of Absolute Stereostructures through Quantum Chemical Circular Dichroism Calculations

2. Time Dependent Density Functional Theory Calculations for Electronic Circular Dichroism Spectra and Optical Rotations of Conformationally Flexible Chiral Donor−Acceptor Dyad

3. VCD Spectroscopy for Organic Chemists

4. Understanding Solvent Effects in Vibrational Circular Dichroism Spectra: [1,1′-Binaphthalene]-2,2′-diol in Dichloromethane, Acetonitrile, and Dimethyl Sulfoxide Solvents

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