Scope, limitations and mechanistic analysis of the HyperBTM-catalyzed acylative kinetic resolution of tertiary heterocyclic alcohols

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

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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A C=O•••isothiouronium interaction dictates enantiodiscrimination in acylative kinetic resolution of tertiary heterocyclic alcohols (dataset 2)
Greenhalgh, M. D. (Creator), Smith, S. (Creator), Walden, D. M. (Creator), Taylor, J. E. (Creator), Brice, Z. (Creator), Robinson, E. (Creator), Fallan, C. (Creator), Cordes, D. B. (Creator), Slawin, A. M. Z. (Creator), Richardson, H. C. (Creator), Grove, M. A. (Creator), Ha-Yeon Cheong, P. (Creator) & Smith, A. D. (Creator), Cambridge Crystallographic Data Centre, 2017
https://dx.doi.org/10.5517/ccdc.csd.cc1pq5k4 and one more link, https://dx.doi.org/10.5517/ccdc.csd.cc1pq5l5 (show fewer)
Dataset
data underpinning "Scope, limitations and mechanistic analysis of the HyperBTM-catalyzed acylative kinetic resolution of tertiary heterocyclic alcohols"
Smith, A. D. (Creator) & Greenhalgh, M. (Contributor), University of St Andrews, 12 Aug 2021
DOI: 10.17630/f069ab41-9f98-438b-83b7-197307dab28d
Dataset

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