Underpinning Mechanistic Studies of NHC-Organocatalysis: A Breslow Intermediate Reactivity Scale

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• data underpinning "a-Phenylthioaldehydes for the effective generation of acyl azolium and azolium enolate intermediates"

  Smith, A. D. (Creator), Majhi, P. (Creator), Zysman-Colman, E. (Creator), Prentice, C. (Creator), Ewing, P. (Creator), Young, C. M. (Creator), Van Rees, K. (Creator) & Arnold, P. (Creator), University of St Andrews, 30 Jul 2024

  DOI: 10.17630/b0dfa038-03b4-4054-a2a3-72a4e1593b16

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• Kinetic and Structure-Activity Studies of the Triazolium Ion- catalyzed Intramolecular Stetter Reaction (dataset)

  Smith, A. D. (Creator) & Young, C. M. (Creator), University of St Andrews, 2 Jun 2021

  DOI: 10.17630/7b18dcdd-72a3-4b26-909b-25ccd31cd58c

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• data underpinning "The Role of the Fused Ring in Bicyclic Triazolium Organocatalysts: Kinetic, X-ray and DFT Insights"

  Smith, A. D. (Creator), Duan, Z. (Owner) & Young, C. M. (Creator), University of St Andrews, 30 Aug 2022

  DOI: 10.17630/5a51a8de-b938-4a46-8f53-ee8c5981166c

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• CCDC 2124937 - 2124950 & 2124952 - 2124958: Experimental Crystal Structure Determination

  Zhu, J. (Creator), Moreno, I. (Creator), Quinn, P. (Creator), Yufit, D. S. (Creator), Song, L. (Creator), Young, C. M. (Creator), Duan, Z. (Creator), Tyler, A. R. (Creator), Waddell, P. G. (Creator), Hall, M. J. (Creator), Probert, M. R. (Creator), Smith, A. D. (Creator) & O’Donoghue, A. C. (Creator), Cambridge Crystallographic Data Centre, 2022

  DOI: 10.5517/ccdc.csd.cc29b5c6, https://dx.doi.org/10.5517/ccdc.csd.cc29b61x and 20 more links, https://dx.doi.org/10.5517/ccdc.csd.cc29b60w, https://dx.doi.org/10.5517/ccdc.csd.cc29b5zt, https://dx.doi.org/10.5517/ccdc.csd.cc29b5ys, https://dx.doi.org/10.5517/ccdc.csd.cc29b5xr, https://dx.doi.org/10.5517/ccdc.csd.cc29b5wq, https://dx.doi.org/10.5517/ccdc.csd.cc29b5vp, https://dx.doi.org/10.5517/ccdc.csd.cc29b5sm, https://dx.doi.org/10.5517/ccdc.csd.cc29b5d7, https://dx.doi.org/10.5517/ccdc.csd.cc29b5f8, https://dx.doi.org/10.5517/ccdc.csd.cc29b5g9, https://dx.doi.org/10.5517/ccdc.csd.cc29b5hb, https://dx.doi.org/10.5517/ccdc.csd.cc29b5jc, https://dx.doi.org/10.5517/ccdc.csd.cc29b5kd, https://dx.doi.org/10.5517/ccdc.csd.cc29b5lf, https://dx.doi.org/10.5517/ccdc.csd.cc29b5mg, https://dx.doi.org/10.5517/ccdc.csd.cc29b5nh, https://dx.doi.org/10.5517/ccdc.csd.cc29b5pj, https://dx.doi.org/10.5517/ccdc.csd.cc29b5qk, https://dx.doi.org/10.5517/ccdc.csd.cc29b5rl, https://dx.doi.org/10.5517/ccdc.csd.cc29b5sm (show fewer)

  Dataset

• data underpinning "Isothiourea-Catalyzed [2+2] Cycloaddition of C(1)-Ammonium Enolates and N-Alkyl Isatins"

  Smith, A. D. (Creator), Kasten, K. (Creator), Young, C. M. (Creator) & Slawin, A. M. Z. (Creator), University of St Andrews, 25 Jul 2022

  DOI: 10.17630/40852daa-0199-41e9-afb0-600a47d25ab9

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• data underpinning "Probing Regio- and Enantioselectivity in the Formal [2+2] Cycloaddi-tion of C(1)-Alkyl Ammonium Enolates with β- and α,β-Substituted Trifluoromethylenones"

  Smith, A. D. (Creator), Wang, Y. (Owner) & Young, C. M. (Owner), University of St Andrews, 17 May 2023

  DOI: 10.17630/ec54103f-32b7-422b-8e9a-f2c1f623065c, http://hdl.handle.net/10023/26954

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• Data underpinning "Isothiourea-Catalysed Enantioselective Synthesis of Phosphonate-Functionalised β-lactones"

  Smith, A. D. (Creator), Platt, F. (Creator) & Cordes, D. B. (Creator), University of St Andrews, 19 Mar 2025

  DOI: 10.17630/a6b1715c-641b-47c2-8a28-d493726f8e5f

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• Data underpinning "Rate and Equilibrium Constants for the Addition of Triazolium Salt derived N-Heterocyclic Carbenes to Heteroaromatic Aldehydes"

  Smith, A. D. (Creator), Duan, Z. (Creator) & Young, C. M. (Creator), University of St Andrews, 30 Nov 2022

  DOI: 10.17630/4e21c331-2fa6-440f-8636-f9ed563bda3c

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