Eduardo Moya - Concepedia

Author

Eduardo Moya

University of Bath

Also Known As

E MOYA, E Moya, E. Moya, Eduardo Moya

Publications

307

Citations

H-Index

Concepts

All Affiliations

University of Bath

About

Eduardo Moya is an author at University of Bath specializing in engineering, biomolecular engineering, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	7	7	184
2	Medicine	3	3	40
3	Natural Sciences	2	2	47
4	Health Sciences	1	1	16
5	Applied Physics	1	1	13

Eduardo Moya

Publications

266

Citations

H-Index

Page 1

	Year	Citations
Chiral bisfunctionalization of substrates: a powerful strategy for the asymmetric synthesis of C2 symmetric compounds and its application to the synthesis of enantiomerically pure trans-1,3-dithiane 1,3-dioxide Varinder K. Aggarwal, Graham Evans, Eduardo Moya, The Journal of Organic Chemistry Chemical EngineeringEngineeringChiral BisfunctionalizationAsymmetric SynthesisAltmetric Attention Score	1992	60
Practical synthesis of the putative polyamine spider toxin FTX: a proposed blocker of voltage-sensitive calcium channels Ian S. Blagbrough, Eduardo Moya Tetrahedron Letters Chemical BiologyPractical SynthesisVoltage-sensitive Calcium ChannelsPharmacologyBiomolecular Engineering	1994	27
Total synthesis of polyamine amide spider toxin argiotoxin-636 by a practical reductive alkylation strategy Ian S. Blagbrough, Eduardo Moya Tetrahedron Letters Spider Toxin Argiotoxin-636EngineeringBiochemistryBioconjugationTotal Synthesis	1995	26
Preparation of Pincer 4-Functionalized 2-Aminomethylbenzo[<i>h</i>]quinoline Ruthenium Catalysts for Ketone Reduction Sarah Facchetti, Václav Jurčı́k, Salvatore Baldino, Organometallics EngineeringEthyl BenzoylacetateOrganic ChemistryChemistryChemical Derivative	2015	24
Practical, convergent total synthesis of polyamine amide spider toxin NSTX-3 Ian S. Blagbrough, Eduardo Moya, Steven Paul Walford Tetrahedron Letters EngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryChemistry	1996	23
Total syntheses of polyamine amides PhTX-4.3.3 and PhTX-3.4.3: Reductive alkylation is a rapid, practical route to philanthotoxins Eduardo Moya, Ian S. Blagbrough Tetrahedron Letters Reductive AlkylationEngineeringPractical RouteOrganic ChemistryTotal Syntheses	1995	22
Total synthesis of modified jstx toxins: reductive alkylation is a practical route to hexahydropyrimidine polyamine amides Mark Ashton, Eduardo Moya, Ian S. Blagbrough Tetrahedron Letters Polyamine AmidesModified Jstx ToxinsEngineeringBioconjugationTotal Synthesis	1995	16
Differential inhibition of Ca2+ channels in mature rat cerebellar Purkinje cells by sFTX-3.3 and FTX-3.3 Jonathan R. B. Dupere, Eduardo Moya, Ian S. Blagbrough, Neuropharmacology Molecular PhysiologyNeurophysiologyNeuroanatomyPhysiologyNeurotransmission	1996	16
Block of high-threshold calcium channels by the synthetic polyamines sFTX-3.3 and FTX-3.3. Timothy M. Norris, Eduardo Moya, Ian S. Blagbrough, Molecular Pharmacology	1996	15
A study of KNbO<sub>3</sub>in the pressure range to 12 GPa using synchrotron radiation Eduardo Moya, T. Tinoco, A. Polian, Ferroelectrics Letters Section Materials ScienceMaterials EngineeringCrystal StructureEngineeringSynchrotron Radiation Research	1997	13

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