Author Institution: Department of Chemistry, The University of Texas at AustinAvailable microwave spectroscopic data, together with new information on nitrocyclopropane, cyclopropyl cyanide, and cyclopropyl methyl ether, have been analyzed to investigate the nature and extent of interaction between the cyclopropyl ring and substituent groups. A comparison is made with the Walsh and other models for the electron distribution in cyclopropane and with recent SCF results. This work has been supported by The Robert A. Welch Foundation
$^{*}$Supported by a grant from the Petroleum Research Fund administered by the American Chemical So...
Author Institution: Department of Chemistry, University of Cincinnati; Department of Chemistry, Univ...
Author Institution: Scientific Laboratory, Ford Motor CompanyThe fundamentals of cyclopropane, cyano...
$^{1}$ J. P. Friend and B. P. Dailey, J. Chem. Phys. 29, 577 (1958). $^{2}$ R. Hoffmann, Tetrahedron...
The complexes of methylcyclopropane$\cdot$hydrogen chloride (MCP$\cdot$HCl), cyclopropane$\cdot$ammo...
The structures of cyclopropane rings which carry σ-acceptor or σ-donor substituents have been studie...
There is considerable evidence that compounds in which a cyclopropane ring is located adjacent to an...
Chemical shifts and coupling constants have been determined from the analysis of proton nuclear magn...
The nature of the bonding in cyclopropane, the smallest and most highly strained carbocyclic ring sy...
$^{1}$ L. S. Bartell and J. P. Guilory, J. Chem. Phys., 43, 647 (1965). $^{2}$ R. H. Schwendeman and...
Author Institution: Department of Chemistry, University of MichiganThe microwave spectra of the cycl...
$^{a}$A. Bhaumik, W. V. F. Brooks, S. C. Dass and K. V. L. N. Sastry Can. J. Chem. 48, 2949 (1970)Au...
The kinetics of (3+2) cycloaddition reactions of 18 different donor-acceptor cyclopropanes with the ...
A survey of the available data on the properties of cyclopropane systems shows that the common assum...
$^{1}$ L.S. Bartell and J.P. Guillory, J. Chem. Phys. 43, 647 (1965).Author Institution: Department ...
$^{*}$Supported by a grant from the Petroleum Research Fund administered by the American Chemical So...
Author Institution: Department of Chemistry, University of Cincinnati; Department of Chemistry, Univ...
Author Institution: Scientific Laboratory, Ford Motor CompanyThe fundamentals of cyclopropane, cyano...
$^{1}$ J. P. Friend and B. P. Dailey, J. Chem. Phys. 29, 577 (1958). $^{2}$ R. Hoffmann, Tetrahedron...
The complexes of methylcyclopropane$\cdot$hydrogen chloride (MCP$\cdot$HCl), cyclopropane$\cdot$ammo...
The structures of cyclopropane rings which carry σ-acceptor or σ-donor substituents have been studie...
There is considerable evidence that compounds in which a cyclopropane ring is located adjacent to an...
Chemical shifts and coupling constants have been determined from the analysis of proton nuclear magn...
The nature of the bonding in cyclopropane, the smallest and most highly strained carbocyclic ring sy...
$^{1}$ L. S. Bartell and J. P. Guilory, J. Chem. Phys., 43, 647 (1965). $^{2}$ R. H. Schwendeman and...
Author Institution: Department of Chemistry, University of MichiganThe microwave spectra of the cycl...
$^{a}$A. Bhaumik, W. V. F. Brooks, S. C. Dass and K. V. L. N. Sastry Can. J. Chem. 48, 2949 (1970)Au...
The kinetics of (3+2) cycloaddition reactions of 18 different donor-acceptor cyclopropanes with the ...
A survey of the available data on the properties of cyclopropane systems shows that the common assum...
$^{1}$ L.S. Bartell and J.P. Guillory, J. Chem. Phys. 43, 647 (1965).Author Institution: Department ...
$^{*}$Supported by a grant from the Petroleum Research Fund administered by the American Chemical So...
Author Institution: Department of Chemistry, University of Cincinnati; Department of Chemistry, Univ...
Author Institution: Scientific Laboratory, Ford Motor CompanyThe fundamentals of cyclopropane, cyano...