Melvyn Giles - Concepedia

Author

Melvyn Giles

AstraZeneca (United Kingdom)

Also Known As

M Giles, M. E. GILES, M. E. Giles, M. GILES, M. Giles, Melvyn E. Giles, Melvyn Giles

Publications

361

Citations

H-Index

Concepts

All Affiliations

AstraZeneca (United Kingdom)The University of Texas at Austin Loughborough University

About

Melvyn Giles is an author at AstraZeneca (United Kingdom) specializing in organic chemistry, chemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	6	6	171
2	Engineering	5	5	110
3	Biochemistry	4	4	132
4	Biomolecular Engineering	4	4	87
5	Chemical Engineering	1	1	23

Melvyn Giles

Publications

329

Citations

H-Index

Page 1

	Year	Citations
Synthesis of strychnine via the Wieland-Gumlich aldehyde P. Magnus, Melvyn Giles, Roger V. Bonnert, Journal of the American Chemical Society Molecular SciencesChemical MeasurementChemical AnalysisDonut IconAltmetric Attention Score	1992	96
Synthesis of strychnine and the Wieland-Gumlich aldehyde P. Magnus, Melvyn Giles, Roger V. Bonnert, Journal of the American Chemical Society Molecular SciencesChemical AnalysisBiochemistryDonut IconNatural Sciences	1993	78
Routes for the Synthesis of (2<i>S</i>)-2-Methyltetrahydropyran-4-one from Simple Optically Pure Building Blocks Kevin R. Anderson, Stéphanie Atkinson, Takahiro Fujiwara, Organic Process Research & Development EngineeringAlkene MetathesisOrganic ChemistryCarbonyl Group-Propylene Oxide	2009	27
Development of a Manufacturing Process for Sibenadet Hydrochloride, the Active Ingredient of Viozan Melvyn Giles, Colin Thomson, Stephen C. Eyley, Organic Process Research & Development	2004	25
A Convergent Synthesis of AR-C123196 Utilising Reaction Between a Cyclic Carbonate and a Phenol for Aryl Alkyl Ether Formation Glyn L. Allsop, Andrea J. Cole, Melvyn Giles, Organic Process Research & Development Chemical EngineeringMedicinal ChemistryPhenolic Hydroxyl GroupEngineeringBiochemistry	2009	23
N-substituted pyrrolidin-3-ones as heterocyclic building blocks. Enantioselective synthesis of 8-epi- and 1,8,8a-triepi-castanospermine Timothy Gallagher, Melvyn Giles, R. S. SUBRAMANIAN, Journal of the Chemical Society Chemical Communications Bioorganic ChemistryEngineeringRegioselective Aldol ReactionOrganic ChemistryChemistry	1992	23
Taxane diterpenes 3: Formation of the eight-membered B-ring by semi-pinacol rearrangement Philip Magnus, Louis J. Diorazio, Timothy J. Donohoe, Tetrahedron EngineeringHeterocyclicBiochemistryNatural SciencesMolecular Biology	1996	21
Synthesis and lithiation of γ,γ-difunctionalised ketene dithioacetals. Access to a new synthetic equivalent of a β-hydroxy-β-lithioacrylate. X-Ray molecular structure of 2-(1,3-dithian-2-ylidenemethyl)-1,3-dithiane Edward K. Dziadulewicz, Melvyn Giles, William O. Moss, Journal of the Chemical Society Perkin Transactions 1 Enantioselective SynthesisEngineeringNatural SciencesNew Synthetic EquivalentDiversity-oriented Synthesis	1989	16
A new approach to the synthesis of the strychnos alkaloids core structure Philip Magnus, Melvyn Giles Tetrahedron Letters Combinatorial ChemistryBiochemistryNatural SciencesNew ApproachOrganic Chemistry	1993	10
A general and efficient route to 6‐methyl‐pyrazin‐2‐yl‐amines: Alkylation of 2,6‐dichloropyrazine <i>via</i> malonate derivatives Paul Colbon, Alison C. Foster, Melvyn Giles, Journal of Heterocyclic Chemistry	2008	10

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