N. D. A. WALSHE - Concepedia

Author

N. D. A. WALSHE

Also Known As

N. D. A. WALSHE, N.D. Walshe, N.D.A Walshe, Nigel D. A. Walshe, Nigel D. Walshe, Nigel D.A Walshe, Nigel D.A. Walshe, Nigel Walshe, Walshe, N.D., Walshe, N.D.A.

Publications

600

Citations

H-Index

Concepts

All Affiliations

Pfizer (United Kingdom)Bangor University

About

N. D. A. WALSHE is an author at Pfizer (United Kingdom) specializing in organic chemistry, pharmacology, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	303
2	Engineering	4	4	119
3	Biochemistry	4	4	156
4	Natural Sciences	2	2	74
5	Education	1	1	10

N. D. A. WALSHE

Publications

584

Citations

H-Index

Page 1

	Year	Citations
Selamectin: a novel broad-spectrum endectocide for dogs and cats B.F. Bishop, C. I. Bruce, N. A. Evans, Veterinary Parasitology MedicineVeterinary SciencePathologySmall Animal Internal MedicinePharmacology	2000	123
Total synthesis of (+)-milbemycin .beta.3 Anthony G. M. Barrett, Robin A. E. Carr, Stephen V. Attwood, The Journal of Organic Chemistry Antimicrobial Drug DiscoveryBioorganic ChemistryDonut IconMedicineAltmetric Attention Score	1986	97
A short synthetic route to the tricyclic guanidinium core of the batzelladine alkaloids Gregory P. Black, P. J. Murphy, N. D. A. WALSHE Tetrahedron HeterocyclicBiochemistryOrganic ChemistryShort Synthetic RouteBatzelladine Alkaloids	1998	56
Full Stereochemical Assignment and Synthesis of the Potent Anthelmintic Pyrrolobenzoxazine Natural Product CJ-12662 Charles Didier, Douglas J. Critcher, N. D. A. WALSHE, The Journal of Organic Chemistry Full Stereochemical AssignmentMedicinal ChemistryPharmaceutical ChemistryBiochemistryNatural Sciences	2004	50
An intramolecular Baylis-Hillman reaction catalysed by secondary amines Gregory P. Black, Francesca Dinon, Silvia Fratucello, Tetrahedron Letters EngineeringOrganic ChemistryIntramolecular Baylis-hillman ReactionCatalysisStereoselective Synthesis	1997	48
Synthesis of the left hand unit of batzelladine F; Revision of the reported relative stereochemistry Gregory P. Black, P. J. Murphy, Andrew J. Thornhill, Tetrahedron Enantioselective SynthesisHeterocyclicBatzelladine FOrganic ChemistryStereoselective Synthesis	1999	37
On the [42]Cycloaddition Approach to Indolo[2,3-a]carbazoles John F. Barry, Timothy W. Wallace, N. D. A. WALSHE Tetrahedron HeterocyclicEngineeringOrganic ChemistryHeterocycle ChemistryBiomolecular Engineering	1995	28
A short synthetic route to the tricyclic guanidinium core of the batzelladine alkaloids Gregory P. Black, P. J. Murphy, N. D. A. WALSHE, Tetrahedron Letters HeterocyclicBiochemistryOrganic ChemistryShort Synthetic RouteBatzelladine Alkaloids	1996	26
Synthesis and reactions of derivatives of 1,7-dioxaspiro[5.5]undec-2-en-4-one Anthony G. M. Barrett, Robin A. E. Carr, Mark A. W. Finch, The Journal of Organic Chemistry Derivative (Chemistry)Molecular SciencesChemical AnalysisDonut IconAltmetric Attention Score	1986	25
Exploration of the biomimetic synthesis of indole-diterpene mycotoxins: an unexpected cascade reaction during the attempted synthesis of emindole SB J. Stephen Clark, James W. Myatt, Claire Wilson, Chemical Communications Key StepBiosynthesisEngineeringNatural Product SynthesisBiochemistry	2003	24

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