Jonathan M. J. Williams, DPhil
Affiliations: | University of Bath | University of Bath, Bath, England, United Kingdom |
Area:
CatalysisWebsite:
http://people.bath.ac.uk/chsjmjw/index.htmlGoogle:
"Jonathan Williams"Bio:
(1964-2019)
https://www.rsc.org/membership-and-community/member-obituaries/professor-jonathan-williams-frsc/
Mean distance: 7.44 | S | N | B | C | P |
Parents
Sign in to add mentor| Steve G. Davies | grad student | Oxford | |
| David A. Evans | post-doc | 1989-1991 | Harvard |
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Publications
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| Dambatta M, Polidano K, Northey A, et al. (2019) Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles Using Alcohols. Chemsuschem |
| Sanz Sharley DD, Williams JM. (2017) Acetic acid as a catalyst for the N-acylation of amines using esters as the acyl source. Chemical Communications (Cambridge, England) |
| Sanz Sharley DD, Williams JM. (2017) A selective hydration of nitriles catalysed by a Pd(OAc)2-based system in water Tetrahedron Letters. 58: 4090-4093 |
| Jones CS, Bull SD, Williams JM. (2016) DBN hexafluorophosphate salts as convenient sulfonylating and phosphonylating agents. Organic & Biomolecular Chemistry. 14: 8452-8456 |
| Marcé P, Lynch J, Blacker AJ, et al. (2015) A mild hydration of nitriles catalysed by copper(ii) acetate. Chemical Communications (Cambridge, England) |
| Marcé P, Lynch J, Blacker AJ, et al. (2015) Conversion of nitroalkanes into carboxylic acids via iodide catalysis in water. Chemical Communications (Cambridge, England) |
| Abou-Shehada S, Teasdale MC, Bull SD, et al. (2015) Lewis acid activation of pyridines for nucleophilic aromatic substitution and conjugate addition. Chemsuschem. 8: 1083-7 |
| Walton JW, Williams JM. (2015) Catalytic SNAr of unactivated aryl chlorides. Chemical Communications (Cambridge, England). 51: 2786-9 |
| Mura MG, De Luca L, Taddei M, et al. (2014) Synthesis of α,β-unsaturated aldehydes based on a one-pot phase-switch dehydrogenative cross-coupling of primary alcohols. Organic Letters. 16: 2586-9 |
| Abou-Shehada S, Williams JM. (2014) Separated tandem catalysis: It's about time. Nature Chemistry. 6: 12-3 |