Alexander C. Weymouth‐Wilson

Author

University of Oxford

Also Known As

Alexander C. Weymouth-Wilson, Alexander C. Weymouth‐Wilson, Alexander Weymouth-Wilson, Weymouth-Wilson, Alexander C.

Publications

Citations

H-Index

Concepts

All Affiliations

University of Oxford Dextra Laboratories (United Kingdom)Toyama University Hospital University of Toyama Summit (United Kingdom)

About

Alexander C. Weymouth‐Wilson is an author at University of Oxford specializing in natural sciences, organic chemistry, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	11	11	323
2	Biochemistry	10	10	307
3	Engineering	9	9	215
4	Biomolecular Engineering	6	6	156
5	Medicine	4	4	177

Alexander C. Weymouth‐Wilson

Publications

446

Citations

H-Index

Page 1

	Year	Citations
Looking glass inhibitors: scalable syntheses of DNJ, DMDP, and (3R)-3-hydroxy-l-bulgecinine from d-glucuronolactone and of l-DNJ, l-DMDP, and (3S)-3-hydroxy-d-bulgecinine from l-glucuronolactone. DMDP inhibits β-glucosidases and β-galactosidases whereas l-DMDP is a potent and specific inhibitor of α-glucosidases Daniel Best, Chen Wang, Alexander C. Weymouth‐Wilson, Tetrahedron Asymmetry Medicinal ChemistryBioorganic ChemistryBiochemistryMedicineNatural Sciences	2010	54
<i>C</i>-Branched Iminosugars: α-Glucosidase Inhibition by Enantiomers of isoDMDP, isoDGDP, and isoDAB–<scp>l</scp>-isoDMDP Compared to Miglitol and Miglustat Sarah F. Jenkinson, Daniel Best, A. Waldo Saville, The Journal of Organic Chemistry Molecular PharmacologyPharmaceutical ScienceBiosynthesisBioorganic ChemistryBiochemistry	2013	48
Enantioselective synthesis of tetrafluorinated ribose and fructose Bruno Linclau, A. James Boydell, Roxana S. Timofte, Organic & Biomolecular Chemistry Pyranose FormEngineeringCyclisation ApproachPerfluoroalkylidene LithiumOrganic Chemistry	2009	41
Inhibition of Nonmammalian Glycosidases by Azetidine Iminosugars Derived from Stable 3,5-Di-<i>O</i>-triflates of Pentoses Gabriel M. J. Lenagh‐Snow, Noelia Araújo, Sarah F. Jenkinson, Organic Letters Specific InhibitionPharmaceutical ChemistryBioorganic ChemistryBiochemistryMedicine	2011	39
Glycosidase Inhibition by All 10 Stereoisomeric 2,5-Dideoxy-2,5-iminohexitols Prepared from the Enantiomers of Glucuronolactone Benjamin James Ayers, Nigel Ngo, Sarah F. Jenkinson, The Journal of Organic Chemistry Bioorganic ChemistryGlycobiologyGlycosidase InhibitionPharmaceutical ChemistryDefinitive Side-by-side Comparison	2012	36
A new approach to cis -chrysanthemic acid John Mann, Alexander C. Weymouth‐Wilson Carbohydrate Research Sustainable SynthesisNew ApproachOrganic ChemistryChemistrySynthetic Chemistry	1992	31
Green aldose isomerisation: 2-C-methyl-1,4-lactones from the reaction of Amadori ketoses with calcium hydroxide David J. Hotchkiss, Raquel G. Soengas, K.V. Booth, Tetrahedron Letters BiosynthesisBioorganic ChemistryEngineeringBiochemistryGreen Aldose Isomerisation	2006	31
Photocatalysed addition of alcohols to 5-substituted 2,5-dihydrofuran-2-ones: novel synthesis of (3′R)-2′,3′-dideoxy-3′-hydroxymethyl nucleosides John Mann, Alexander C. Weymouth‐Wilson Journal of the Chemical Society Perkin Transactions 1 Derivative (Chemistry)-2′,3′-Dideoxy-3′-hydroxymethyl NucleosidesEngineeringPhotoredox ProcessPhotochemistry	1994	27
Large scale synthesis of the acetonides of l-glucuronolactone and of l-glucose: easy access to l-sugar chirons Alexander C. Weymouth‐Wilson, Robert A. Clarkson, Nigel A. Jones, Tetrahedron Letters BiosynthesisBioorganic ChemistryLarge Scale SynthesisBiochemistryEngineering	2009	27
High yield protection of alcohols, including tertiary and base sensitive alcohols, as benzhydryl ethers by heating with diphenyldiazomethane in the absence of any other reagent Daniel Best, Sarah F. Jenkinson, Sebastian D. Rule, Tetrahedron Letters Benzhydryl EthersChemical EngineeringHigh Yield ProtectionBase Sensitive AlcoholsEngineering	2008	24

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