Cite
Cu-Catalyzed aromatic C–H imidation with N-fluorobenzenesulfonimide: mechanistic details and predictive models† †Electronic supplementary information (ESI) available: (1) CuIBr oxidation by NFSI; (2) details of the Br/F exchange process; (3) bimetallic oxidation of LCuIX (where X = F, Br, Cl, and I) by NFSI; (4) conformational analysis of the oxidation of D3-N-3F; (5) NBO analysis of the Cu2F2 dimer; (6) analysis of electronic states along the catalytic cycle; (7) energy scan for the deprotonation step; (8) isotope effect calculation; (9) calculation procedure to predict regioselectivity for C–H imidation; (10) kinetic profiles of product formation of pre-catalysts; (11) characterization data, 1H and 13C NMR spectra; (12) observation of the proposed intermediate D3-N-3F; (13) energies and Cartesian coordinates. See DOI: 10.1039/c6sc04145k Click here for additional data file
MLA
Haines, Brandon E., et al. “Cu-Catalyzed Aromatic C–H Imidation with N-Fluorobenzenesulfonimide: Mechanistic Details and Predictive Models† †Electronic Supplementary Information (ESI) Available: (1) CuIBr Oxidation by NFSI; (2) Details of the Br/F Exchange Process; (3) Bimetallic Oxidation of LCuIX (Where X = F, Br, Cl, and I) by NFSI; (4) Conformational Analysis of the Oxidation of D3-N-3F; (5) NBO Analysis of the Cu2F2 Dimer; (6) Analysis of Electronic States along the Catalytic Cycle; (7) Energy Scan for the Deprotonation Step; (8) Isotope Effect Calculation; (9) Calculation Procedure to Predict Regioselectivity for C–H Imidation; (10) Kinetic Profiles of Product Formation of Pre-Catalysts; (11) Characterization Data, 1H and 13C NMR Spectra; (12) Observation of the Proposed Intermediate D3-N-3F; (13) Energies and Cartesian Coordinates. See DOI: 10.1039/C6sc04145k Click Here for Additional Data File.” Chemical Science, vol. 8, no. 2, Oct. 2016, pp. 988–1001. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid..........0545ea3f5330cb9259574a8fe049a9c9&authtype=sso&custid=ns315887.
APA
Haines, B. E., Kawakami, T., Kuwata, K., Murakami, K., Itami, K., & Musaev, D. G. (2016). Cu-Catalyzed aromatic C–H imidation with N-fluorobenzenesulfonimide: mechanistic details and predictive models† †Electronic supplementary information (ESI) available: (1) CuIBr oxidation by NFSI; (2) details of the Br/F exchange process; (3) bimetallic oxidation of LCuIX (where X = F, Br, Cl, and I) by NFSI; (4) conformational analysis of the oxidation of D3-N-3F; (5) NBO analysis of the Cu2F2 dimer; (6) analysis of electronic states along the catalytic cycle; (7) energy scan for the deprotonation step; (8) isotope effect calculation; (9) calculation procedure to predict regioselectivity for C–H imidation; (10) kinetic profiles of product formation of pre-catalysts; (11) characterization data, 1H and 13C NMR spectra; (12) observation of the proposed intermediate D3-N-3F; (13) energies and Cartesian coordinates. See DOI: 10.1039/c6sc04145k Click here for additional data file. Chemical Science, 8(2), 988–1001.
Chicago
Haines, Brandon E., Takahiro Kawakami, Keiko Kuwata, Kei Murakami, Kenichiro Itami, and Djamaladdin G. Musaev. 2016. “Cu-Catalyzed Aromatic C–H Imidation with N-Fluorobenzenesulfonimide: Mechanistic Details and Predictive Models† †Electronic Supplementary Information (ESI) Available: (1) CuIBr Oxidation by NFSI; (2) Details of the Br/F Exchange Process; (3) Bimetallic Oxidation of LCuIX (Where X = F, Br, Cl, and I) by NFSI; (4) Conformational Analysis of the Oxidation of D3-N-3F; (5) NBO Analysis of the Cu2F2 Dimer; (6) Analysis of Electronic States along the Catalytic Cycle; (7) Energy Scan for the Deprotonation Step; (8) Isotope Effect Calculation; (9) Calculation Procedure to Predict Regioselectivity for C–H Imidation; (10) Kinetic Profiles of Product Formation of Pre-Catalysts; (11) Characterization Data, 1H and 13C NMR Spectra; (12) Observation of the Proposed Intermediate D3-N-3F; (13) Energies and Cartesian Coordinates. See DOI: 10.1039/C6sc04145k Click Here for Additional Data File.” Chemical Science 8 (2): 988–1001. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid..........0545ea3f5330cb9259574a8fe049a9c9&authtype=sso&custid=ns315887.