المؤلفون: Vink, Matthias J.A., van Geenen, Fred A.M.G., Berden, Giel, O’Riordan, Timothy J. C., Howe, Peter W.A., Oomens, Jos, Perry, Simon J., Martens, Jonathan

المساهمون: H2020 Future and Emerging Technologies, Nederlandse Organisatie voor Wetenschappelijk Onderzoek

المصدر: Environmental Science & Technology ; volume 56, issue 22, page 15563-15572 ; ISSN 0013-936X 1520-5851

مصطلحات موضوعية: Environmental Chemistry, General Chemistry

الإتاحة: https://doi.org/10.1021/acs.est.2c03210Test

المؤلفون: Hartley, Will C., O'Riordan, Timothy J. C., Smith, Andrew D.

المصدر: Hartley , W C , O'Riordan , T J C & Smith , A D 2017 , ' Aryloxide-promoted catalyst turnover in Lewis base organocatalysis ' , Synthesis , vol. 49 , no. 15 , pp. 3303-3310 . https://doi.org/10.1055/s-0036-1589047Test

مصطلحات موضوعية: Lewis base catalysis, catalyst turnover and release, Aryloxide, Isothiourea, NHC, Tertiary amines

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/aryloxidepromoted-catalyst-turnover-in-lewis-base-organocatalysisTest(ee72c858-a734-4d86-aa6d-83c7c20bd48a).html

الإتاحة: https://doi.org/10.1055/s-0036-1589047Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/aryloxidepromoted-catalyst-turnover-in-lewis-base-organocatalysisTest(ee72c858-a734-4d86-aa6d-83c7c20bd48a).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/14646/1/Smith_2017_Synthesis_Aryloxide_AAM.pdfTest

المؤلفون: Stark, Daniel Graham, Williamson, Patrick, Gayner, Emma R, Musolino, Stefania Francesca, Kerr, Ryan William Frederick, Taylor, James Edward, Slawin, Alexandra Martha Zoya, O'Riordan, Timothy J C, Macgregor, Stuart A, Smith, Andrew David

المصدر: Stark , D G , Williamson , P , Gayner , E R , Musolino , S F , Kerr , R W F , Taylor , J E , Slawin , A M Z , O'Riordan , T J C , Macgregor , S A & Smith , A D 2016 , ' Isothiourea-catalysed enantioselective pyrrolizine synthesis : synthetic and computational studies ' , Organic & Biomolecular Chemistry , vol. 14 , no. 38 , pp. 8957-8965 . https://doi.org/10.1039/C6OB01557CTest

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/isothioureacatalysed-enantioselective-pyrrolizine-synthesisTest(df25d7fa-3866-4593-a3f8-5538ca04a20e).html

الإتاحة: https://doi.org/10.1039/C6OB01557CTest
https://research-portal.st-andrews.ac.uk/en/researchoutput/isothioureacatalysed-enantioselective-pyrrolizine-synthesisTest(df25d7fa-3866-4593-a3f8-5538ca04a20e).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/9335/1/ADS_OrgBioChem_c6ob01557c_CCBY.pdfTest
http://www.rsc.org/suppdata/c6/ob/c6ob01557c/c6ob01557c1.zipTest
http://www.rsc.org/suppdata/c6/ob/c6ob01557c/c6ob01557c2.pdfTest

المؤلفون: Stark, Daniel Graham, Young, Claire Mary, O'Riordan, Timothy J C, Slawin, Alexandra Martha Zoya, Smith, Andrew David

المصدر: Stark , D G , Young , C M , O'Riordan , T J C , Slawin , A M Z & Smith , A D 2016 , ' Enantioselective isothiourea-catalysed trans -dihydropyridinone synthesis using saccharin-derived ketimines : scope and limitations ' , Organic & Biomolecular Chemistry , vol. 14 , no. 34 , pp. 8068-8073 . https://doi.org/10.1039/C6OB01473ATest

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/enantioselective-isothioureacatalysed-transdihydropyridinone-synthesis-using-saccharinderived-ketiminesTest(aa8bd179-6ffe-44f5-a791-a64dc27659d9).html

الإتاحة: https://doi.org/10.1039/C6OB01473ATest
https://research-portal.st-andrews.ac.uk/en/researchoutput/enantioselective-isothioureacatalysed-transdihydropyridinone-synthesis-using-saccharinderived-ketiminesTest(aa8bd179-6ffe-44f5-a791-a64dc27659d9).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/9332/1/Stark_2016_OBCc6ob01473a_CCBY.pdfTest
http://www.rsc.org/suppdata/c6/ob/c6ob01473a/c6ob01473a1.pdfTest

المؤلفون: Stark, Daniel G., Morrill, Louis C., Cordes, David B., Slawin, Alexandra M. Z., O'Riordan, Timothy J. C., Smith, Andrew D.

المساهمون: Royal Society for a University Research Fellowship (ADS), Syngenta, European Union's Seventh Framework Programme

المصدر: Chemistry – An Asian Journal ; volume 11, issue 3, page 395-400 ; ISSN 1861-4728 1861-471X

الإتاحة: https://doi.org/10.1002/asia.201500907Test

المؤلفون: Stark, Daniel Graham, O’Riordan, Timothy J. C., Smith, Andrew David

المصدر: Stark , D G , O’Riordan , T J C & Smith , A D 2014 , ' Synthesis of di-, tri-, and tetrasubstituted pyridines from (phenylthio)carboxylic acids and 2-[aryl(tosylimino)methyl]acrylates ' , Organic Letters , vol. 16 , no. 24 , pp. 6496-6499 . https://doi.org/10.1021/ol503360qTest

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/synthesis-of-di-tri-and-tetrasubstituted-pyridines-from-phenylthiocarboxylic-acids-and-2aryltosyliminomethylacrylatesTest(c91e152e-4141-4e04-ba20-1a92bc53a168).html

الإتاحة: https://doi.org/10.1021/ol503360qTest
https://research-portal.st-andrews.ac.uk/en/researchoutput/synthesis-of-di-tri-and-tetrasubstituted-pyridines-from-phenylthiocarboxylic-acids-and-2aryltosyliminomethylacrylatesTest(c91e152e-4141-4e04-ba20-1a92bc53a168).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/7896/1/DGS_ADS_Pyridines_Org_Lett_Final.pdfTest

المؤلفون: Stark, Daniel G., Morrill, Louis C., Yeh, Pei‐Pei, Slawin, Alexandra M. Z., O'Riordan, Timothy J. C., Smith, Andrew D.

المصدر: Angewandte Chemie International Edition ; volume 52, issue 44, page 11642-11646 ; ISSN 1433-7851 1521-3773

الإتاحة: https://doi.org/10.1002/anie.201306786Test

المؤلفون: Stark, Daniel G., Williamson, Patrick, Gayner, Emma R., Musolino, Stefania F., Kerr, Ryan W. F., Taylor, James E., Slawin, Alexandra M. Z., O'Riordan, Timothy J. C., Macgregor, Stuart A., Smith, Andrew D.

المصدر: Organic & Biomolecular Chemistry

مصطلحات موضوعية: Chemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::ec06a04c197b692ae13bfb58979ceaabTest
http://europepmc.org/articles/PMC5314687Test

المؤلفون: Hartley, Will C., O'Riordan, Timothy J. C., Smith, Andrew D.

المساهمون: European Commission, EPSRC, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: Lewis base catalysis, catalyst turnover and release, Aryloxide, Isothiourea, NHC, Tertiary amines, QD Chemistry, QD

وصف الملف: application/pdf

العلاقة: Synthesis; Hartley , W C , O'Riordan , T J C & Smith , A D 2017 , ' Aryloxide-promoted catalyst turnover in Lewis base organocatalysis ' , Synthesis , vol. 49 , no. 15 , pp. 3303-3310 . https://doi.org/10.1055/s-0036-1589047Test; PURE: 249974102; PURE UUID: ee72c858-a734-4d86-aa6d-83c7c20bd48a; Scopus: 85021301415; WOS: 000406065500017; http://hdl.handle.net/10023/14646Test; https://doi.org/10.1055/s-0036-1589047Test; N/A; EP/L016419/1; WM140071

الإتاحة: https://doi.org/10.1055/s-0036-1589047Test
http://hdl.handle.net/10023/14646Test

المؤلفون: Stark, Daniel G., Morrill, Louis C., Cordes, David B., Slawin, Alexandra M. Z., O'Riordan, Timothy J. C., Smith, Andrew D.

المصدر: ChemInform ; volume 47, issue 25 ; ISSN 0931-7597 1522-2667

الإتاحة: https://doi.org/10.1002/chin.201625029Test