David M. Hollinshead

Author

AstraZeneca (United Kingdom)

Also Known As

D. M. HOLLINSHEAD, D. M. Hollinshead, David Hollinshead, David M Hollinshead, David M. Hollinshead

Publications

648

Citations

H-Index

Concepts

All Affiliations

AstraZeneca (United Kingdom)Imperial College London

About

David M. Hollinshead is an author at AstraZeneca (United Kingdom) specializing in organic chemistry, engineering, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	11	11	526
2	Natural Sciences	7	7	292
3	Biomolecular Engineering	6	6	242
4	Biochemistry	5	5	194
5	Medicine	3	3	70

David M. Hollinshead

Publications

644

Citations

H-Index

Page 1

	Year	Citations
The Diels–Alder route to drimane related sesquiterpenes; synthesis of cinnamolide, polygodial, isodrimeninol, drimenin and warburganal David M. Hollinshead, S. C. Howell, Steven V. Ley, Journal of the Chemical Society Perkin Transactions 1 Diels–alder RouteParent DieneBioorganic ChemistryEngineeringBiochemistry	1983	109
Oxo complexes of ruthenium(<scp>VI</scp>) and (<scp>VII</scp>) as organic oxidants Graham Green, William P. Griffith, David M. Hollinshead, Journal of the Chemical Society Perkin Transactions 1 Inorganic ChemistryChemical EngineeringOxo ComplexesEngineeringCoordination Complex	1984	101
Enantioselective Synthesis of 3,6-Dihydro-1<i>H</i>-pyridin-2-ones: Unexpected Regioselectivity in the Palladium-Catalyzed Decarboxylative Carbonylation of 5-Vinyloxazolidin-2-ones Julian G. Knight, Simon W. Ainge, Andrew M. Harm, Journal of the American Chemical Society Chemical EngineeringUk Zeneca PharmaceuticalsEngineeringEnantioselective SynthesisNatural Sciences	2000	73
Synthesis of β-lactams from π-allyltricarbonyliron (lactone) complexes Gary D. Annis, E. M. HEBBLETHWAITE, Simon T. Hodgson, Journal of the Chemical Society Perkin Transactions 1 β-Lactam CompoundsLactam ComplexesChemical EngineeringEngineeringOrganic Chemistry	1983	43
Fe2(co)g in tetrahydrofuran or under sonochemical conditions as convenient practical routes to π-allyltricarbonyliron lactone complexes Averil M. Horton, David M. Hollinshead, Steven V. Ley Tetrahedron Inorganic ChemistryChemical EngineeringEngineeringConvenient Practical RoutesCoordination Complex	1984	41
Dissolving metal reduction of esters to alkanes. A method for the deoxygenation of alcohols Anthony G. M. Barrett, Christopher R. A. Godfrey, David M. Hollinshead, Journal of the Chemical Society Perkin Transactions 1 Chemical EngineeringSelective DeoxygenationEngineeringRadical (Chemistry)Organic Chemistry	1981	40
Synthesis of the β-lactam antibiotic (+)- thienamycin via an intermediate π-allyltricarbonyliron lactone complex Simon T. Hodgson, David M. Hollinshead, Steven V. Ley Tetrahedron EngineeringBioorganic ChemistryOrganic ChemistryPharmacologySynthetic Chemistry	1985	38
Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters Seth J. Parker, Joel Encarnación-Rosado, Kate E.R. Hollinshead, Nature Communications	2021	36
Dispiroketals in Synthesis (Part 3):<sup>1</sup>Selective Protection of Diequatorial Vicinal Diols in Carbohydrates Steven V. Ley, Geert‐Jan Boons, Ray Leslie, Synthesis Bioorganic ChemistrySelective ProtectionGlycobiologyOrganic ChemistryPolysaccharide	1993	29
π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin Simon T. Hodgson, David M. Hollinshead, Steven V. Ley Journal of the Chemical Society Chemical Communications Medicinal ChemistryEngineeringπ-Allyltricarbonyliron Lactone ComplexesSuitable ElaborationNatural Sciences	1984	25

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