المؤلفون: Veenboer, Richard M. P., Collado, Alba, Dupuy, Stephanie, Lebl, Tomas, Falivene, Laura, Cavallo, Luigi, Cordes, David B., Slawin, Alexandra M. Z., Cazin, Catherine S. J., Nolan, Steven P.

المصدر: Veenboer , R M P , Collado , A , Dupuy , S , Lebl , T , Falivene , L , Cavallo , L , Cordes , D B , Slawin , A M Z , Cazin , C S J & Nolan , S P 2017 , ' Inner-sphere versus outer-sphere coordination of BF 4 - in a NHC-gold(I) complex ' , Organometallics , vol. 36 , no. 15 , pp. 2861-2869 . https://doi.org/10.1021/acs.organomet.7b00345Test

مصطلحات موضوعية: N-heterocyclic carbene, Silver-free protocols, Gold catalysis, Gold(III) complexes, Reaction-mechanism, Highly efficient, Stereoselective hydrocarboxylation, Alkynes, Counterion, NHC

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/innersphere-versus-outersphere-coordination-of-bf4-in-a-nhcgoldi-complexTest(98dcaf3f-6342-41bf-82cf-7508ef5aa8c3).html

الإتاحة: https://doi.org/10.1021/acs.organomet.7b00345Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/innersphere-versus-outersphere-coordination-of-bf4-in-a-nhcgoldi-complexTest(98dcaf3f-6342-41bf-82cf-7508ef5aa8c3).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/15622/1/Cordes_2017_Organometallics_NHC_gold_I_complex_AAM.pdfTest

المؤلفون: Trose, Michael, Lazreg, Faima, Chang, Tao, Nahra, Fady, Cordes, David B, Slawin, Alexandra MZ, Cazin, Catherine

المصدر: ACS CATALYSIS ; ISSN: 2155-5435

مصطلحات موضوعية: Chemistry, N-heterocyclic carbenes, copper(I), hydrosilylation, ketones, dinuclear, N-HETEROCYCLIC CARBENE, COPPER-CATALYZED HYDROALKYLATION, TRINUCLEAR COPPER(I), CARBONYL-COMPOUNDS, LIGANDS, ALKYNES, REACTIVITY, HYDRIDE, SUBSTITUTION, TETRANUCLEAR

وصف الملف: application/pdf

العلاقة: https://biblio.ugent.be/publication/8536976Test; http://hdl.handle.net/1854/LU-8536976Test; http://dx.doi.org/10.1021/acscatal.6b02723Test; https://biblio.ugent.be/publication/8536976/file/8555533Test

الإتاحة: https://doi.org/10.1021/acscatal.6b02723Test
https://biblio.ugent.be/publication/8536976Test
http://hdl.handle.net/1854/LU-8536976Test
https://biblio.ugent.be/publication/8536976/file/8555533Test

المؤلفون: Veenboer, Richard M. P., Collado, Alba, Dupuy, Stephanie, Lebl, Tomas, Falivene, Laura, Cavallo, Luigi, Cordes, David B., Slawin, Alexandra M. Z., Cazin, Catherine S. J., Nolan, Steven P.

المساهمون: University of St Andrews. EaSTCHEM, University of St Andrews. School of Chemistry

مصطلحات موضوعية: N-heterocyclic carbene, Silver-free protocols, Gold catalysis, Gold(III) complexes, Reaction-mechanism, Highly efficient, Stereoselective hydrocarboxylation, Alkynes, Counterion, NHC, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Organometallics; 251051913; 98dcaf3f-6342-41bf-82cf-7508ef5aa8c3; 000407869100019; 85027407578; Veenboer , R M P , Collado , A , Dupuy , S , Lebl , T , Falivene , L , Cavallo , L , Cordes , D B , Slawin , A M Z , Cazin , C S J & Nolan , S P 2017 , ' Inner-sphere versus outer-sphere coordination of BF 4 - in a NHC-gold(I) complex ' , Organometallics , vol. 36 , no. 15 , pp. 2861-2869 . https://doi.org/10.1021/acs.organomet.7b00345Test; ORCID: /0000-0002-0269-3221/work/48131717; ORCID: /0000-0002-5366-9168/work/36874686; ORCID: /0000-0002-9527-6418/work/56861708; https://hdl.handle.net/10023/15622Test

الإتاحة: https://doi.org/10.1021/acs.organomet.7b00345Test
https://hdl.handle.net/10023/15622Test

المؤلفون: Nahra, Fady, Patrick, Scott R, Bello, Davide, Brill, Marcel, Obled, Alan, Cordes, David B, Slawin, Alexandra M Z, O'Hagan, David, Nolan, Steven P

المصدر: Chemcatchem

مصطلحات موضوعية: carbenes, bifluorides, hydrofluorination, gold, alkynes, Communications

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::a335ce5a37d68cf1452529f22fc75725Test
http://europepmc.org/articles/PMC4515107Test

المؤلفون: Brill, Marcel, Nahra, Fady, Gomez-Herrera, Alberto, Zinser, Caroline, Cordes, David B., Slawin, Alexandra M. Z., Nolan, Steven P.

المصدر: Brill , M , Nahra , F , Gomez-Herrera , A , Zinser , C , Cordes , D B , Slawin , A M Z & Nolan , S P 2017 , ' Gold-N-Heterocyclic Carbene Complexes of Mineral Acids ' , ChemCatChem , vol. 9 , no. 1 , pp. 117-120 . https://doi.org/10.1002/cctc.201601290Test

مصطلحات موضوعية: MEYER-SCHUSTER REARRANGEMENT, ONE-POT SYNTHESIS, MECHANISTIC INSIGHTS, SILVER-FREE, CATALYSIS, ALKYNES, COUNTERION, HYDRATION, REACTIVITY, ALCOHOLS

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/goldnheterocyclic-carbene-complexes-of-mineral-acidsTest(a2cb6331-b25c-4fd6-8636-d5eaed5e0ab0).html

الإتاحة: https://doi.org/10.1002/cctc.201601290Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/goldnheterocyclic-carbene-complexes-of-mineral-acidsTest(a2cb6331-b25c-4fd6-8636-d5eaed5e0ab0).html

المؤلفون: Veenboer, Richard M. P., Gasperini, Danila, Nahra, Fady, Cordes, David B, Slawin, Alexandra MZ, Cazin, Catherine, Nolan, Steven

المصدر: ORGANOMETALLICS ; ISSN: 0276-7333 ; ISSN: 1520-6041

مصطلحات موضوعية: Chemistry, N-HETEROCYCLIC CARBENE, SILVER-FREE PROTOCOLS, GOLD CATALYSIS, CHEMICAL-SHIFTS, NHC COMPLEXES, REACTIVITY, VERSATILE, ADDUCTS, ALKYNES, ACID

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://biblio.ugent.be/publication/8536734Test; http://hdl.handle.net/1854/LU-8536734Test; http://dx.doi.org/10.1021/acs.organomet.7b00622Test; https://biblio.ugent.be/publication/8536734/file/8536735Test

الإتاحة: https://doi.org/10.1021/acs.organomet.7b00622Test
https://biblio.ugent.be/publication/8536734Test
http://hdl.handle.net/1854/LU-8536734Test
https://biblio.ugent.be/publication/8536734/file/8536735Test

المؤلفون: Gõmez-Suárez, Adrián, Oonishi, Yoshihiro, Martin, Anthony R., Vummaleti, Sai V.C., Nelson, David J., Cordes, David B., Slawin, Alexandra M.Z., Cavallo, Luigi, Nolan, Steven P., Poater, Albert

المصدر: Gõmez-Suárez , A , Oonishi , Y , Martin , A R , Vummaleti , S V C , Nelson , D J , Cordes , D B , Slawin , A M Z , Cavallo , L , Nolan , S P & Poater , A 2016 , ' On the mechanism of the digold(I)-hydroxide-catalysed hydrophenoxylation of alkynes ' , Chemistry - A European Journal , vol. 22 , no. 3 , pp. 1125-1132 . https://doi.org/10.1002/chem.201503097Test

مصطلحات موضوعية: Alkynes, Density functional calculations, Gold, Homogeneous catalysis, Hydrophenoxylation, Reaction mechanisms

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/on-the-mechanism-of-the-digoldihydroxidecatalysed-hydrophenoxylation-ofTest-alkynes(e4e0d7a4-adbe-4e62-8e1e-d9cac7d5d6a7).html

الإتاحة: https://doi.org/10.1002/chem.201503097Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/on-the-mechanism-of-the-digoldihydroxidecatalysed-hydrophenoxylation-ofTest-alkynes(e4e0d7a4-adbe-4e62-8e1e-d9cac7d5d6a7).html

المؤلفون: Nahra, Fady, Patrick, Scott R, Bello, Davide, Brill, Marcel, Obled, Alan, Cordes, David B, Slawin, Alexandra MZ, O'Hagan, David, Nolan, Steven

المصدر: CHEMCATCHEM ; ISSN: 1867-3880

مصطلحات موضوعية: Chemistry, alkynes, bifluorides, gold, hydrofluorination, carbenes, C-H FLUORINATION, COPPER-MEDIATED FLUORINATION, NUCLEOPHILIC FLUORINATION, UNACTIVATED ALKENES, FLUORIDE COMPLEX, BOND ACTIVATION, ARYL BROMIDES, REACTIVITY, LIGANDS, REAGENT

العلاقة: https://biblio.ugent.be/publication/8168399Test; http://hdl.handle.net/1854/LU-8168399Test; http://dx.doi.org/10.1002/cctc.201402891Test

الإتاحة: https://doi.org/10.1002/cctc.201402891Test
https://biblio.ugent.be/publication/8168399Test
http://hdl.handle.net/1854/LU-8168399Test

المؤلفون: Gómez-Suárez, Adrián, Oonishi, Yoshihiro, Martin, Anthony R., Vummaleti, Sai V. C., Nelson, David J., Cordes, David B., Slawin, Alexandra M. Z., Cavallo, Luigi, Nolan, Steven P., Poater, Albert

المساهمون: Chemical Science Program, KAUST Catalysis Center (KCC), Physical Science and Engineering (PSE) Division, EaStCHEM School of Chemistry, University of St. Andrews, North Haugh St. Andrews, Fife KY16 9ST UK, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812 Japan, Institut de Chimie de Nice, UMR 7272, Université de Nice Sophia Antipolis, CNRS, Parc Valrose 06108 Nice cedex 2 France, WestCHEM Department of Pure & Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street Glasgow G1 1XL UK, Chemistry Department, College of Science, King Saud University, P.O. Box 2455 Riyadh 11451 Saudi Arabia, Institut de Química Computacional i Catàlisi and Departament de Química, Universitat de Girona, Campus Montilivi 17071 Girona, Catalonia Spain

مصطلحات موضوعية: Alkynes, Density functional calculations, Gold, Homogeneous catalysis, Hydrophenoxylation, Reaction mechanisms

وصف الملف: application/pdf

العلاقة: https://strathprints.strath.ac.uk/54558/1/Gomez_Suarez_etal_CEJ_2015_On_the_mechanism_of_the_digold_I_hydroxide_catalyzed.pdfTest; Gómez-Suárez A, Oonishi Y, Martin AR, Vummaleti SVC, Nelson DJ, et al. (2015) On the Mechanism of the Digold(I)-Hydroxide-Catalysed Hydrophenoxylation of Alkynes. Chem Eur J 22: 1125–1132. Available: http://dx.doi.org/10.1002/chem.201503097Test.; Chemistry - A European Journal; http://hdl.handle.net/10754/621705Test

الإتاحة: https://doi.org/10.1002/chem.201503097Test
https://doi.org/10.5517/ccdc.csd.cc13kz2qTest
http://hdl.handle.net/10754/621705Test

المؤلفون: Tran, Anthony T.¹, Huynh, Vincent A.¹, Friz, Emily M.¹, Whitney, Sara K.¹, Cordes, David B. cordes@pacificu.edu

المصدر: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Apr2009, Vol. 50 Issue 16, p1817-1819. 3p.

مصطلحات موضوعية: *CHEMICAL reduction, *ALKENES, *ALKYNES, *SODIUM borohydride, *ACETIC acid, *PALLADIUM catalysts