Emulating nature: Reaction diversity and understanding through asymmetric catalysis

Smith, Andrew David (PI)

School of Chemistry

Project: Standard

Acronym	ERC Starting Grant EnolCat
Status	Finished
Effective start/end date	1/10/11 → 30/06/17

Funding

European Commission: £1,211,963.97

40 Article
1 Review article

Scope, limitations and mechanistic analysis of the HyperBTM-catalyzed acylative kinetic resolution of tertiary heterocyclic alcohols
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., 11 Jan 2022, In: European Journal of Organic Chemistry. p. 30-43 14 p., e202101111.
Research output: Contribution to journal › Article › peer-review

Open Access
File
Isothiourea-catalyzed enantioselective α-alkylation of esters via 1,6-conjugate addition to para-quinone methides
Arokianathar, J. N., Hartley, W., McLaughlin, C., Greenhalgh, M. D., Stead, D., Ng, S., Slawin, A. M. Z. & Smith, A. D., 20 Oct 2021, In: Molecules. 26, 21, 13 p., 6333.
Research output: Contribution to journal › Article › peer-review

Open Access
File
Isothiourea-catalyzed acylative kinetic resolution of tertiary α-hydroxy esters
Qu, S., Smith, S., Laina-Martin, V., Neyyappadath, R., Greenhalgh, M. D. & Smith, A. D., 14 Sept 2020, In: Angewandte Chemie International Edition. 59, 38, p. 16572-16578 8 p.
Research output: Contribution to journal › Article › peer-review

Open Access
File