المؤلفون: Smith, Samuel, Greenhalgh, Mark D., Feoktistova, Taisiia, Walden, Daniel M., Taylor, James E., Cordes, David B., Slawin, Alexandra M. Z., Cheong, Paul Ha-Yeon, Smith, Andrew D.

المساهمون: European Commission, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: Kinetic resolution, Enantioselectivity, Acyl transfer, Organocatalysis, Tertiary alcohol, QD Chemistry, DAS, MCC, QD

وصف الملف: application/pdf

العلاقة: European Journal of Organic Chemistry; 276154021; 0042408d-7c39-4310-b3a7-d60d1bdb2668; 85118824423; 000717013700001; Smith , S , Greenhalgh , M D , Feoktistova , T , Walden , D M , Taylor , J E , Cordes , D B , Slawin , A M Z , Cheong , P H-Y & Smith , A D 2022 , ' Scope, limitations and mechanistic analysis of the HyperBTM-catalyzed acylative kinetic resolution of tertiary heterocyclic alcohols ' , European Journal of Organic Chemistry , pp. 30-43 . https://doi.org/10.1002/ejoc.202101111Test; ORCID: /0000-0002-2104-7313/work/103510852; ORCID: /0000-0002-9527-6418/work/103510915; ORCID: /0000-0002-5366-9168/work/103510944; https://hdl.handle.net/10023/26371Test; N/A; WM140071

الإتاحة: https://doi.org/10.1002/ejoc.202101111Test
https://hdl.handle.net/10023/26371Test

المؤلفون: Greenhalgh, Mark D., Smith, Samuel M., Walden, Daniel M., Taylor, James E., Brice, Zamira, Robinson, Emily R. T., Fallan, Charlene, Cordes, David B., Slawin, Alexandra M. Z., Richardson, H. Camille, Grove, Markas A., Cheong, Paul Ha-Yeon, Smith, Andrew D.

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

مصطلحات موضوعية: Acylation, Kinetic resolution, Lewis bases, Organocatalysis, Tertiary alcohols, QD Chemistry, DAS, BDC, R2C, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 252045715; d1b5cdb2-e2b0-405b-b952-a05053a6d2c7; 85042110491; 000426759900035; Greenhalgh , M D , Smith , S M , Walden , D M , Taylor , J E , Brice , Z , Robinson , E R T , Fallan , C , Cordes , D B , Slawin , A M Z , Richardson , H C , Grove , M A , Cheong , P H-Y & Smith , A D 2018 , ' A C=O•••isothiouronium interaction dictates enantiodiscrimination in acylative kinetic resolution of tertiary heterocyclic alcohols ' , Angewandte Chemie International Edition , vol. 57 , no. 12 , pp. 3200-3206 . https://doi.org/10.1002/anie.201712456Test; ORCID: /0000-0002-2104-7313/work/42023858; ORCID: /0000-0002-5366-9168/work/42023872; ORCID: /0000-0002-9527-6418/work/56861440; https://hdl.handle.net/10023/17091Test; WM140071; N/A

الإتاحة: https://doi.org/10.1002/anie.201712456Test
https://hdl.handle.net/10023/17091Test