A. J. DUGGAN - Concepedia

Author

A. J. DUGGAN

La Roche College

Also Known As

A. J. DUGGAN, A. J. Duggan, A. J. S. DUGGAN, Angelina J. Duggan, Angelina J. Serio Duggan, Angelina J.Duggan

Publications

260

Citations

H-Index

Concepts

All Affiliations

La Roche College Roche (Switzerland)Merck & Co., Inc., Rahway, NJ, USA (United States)

About

A. J. DUGGAN is an author at La Roche College specializing in chemistry, organic chemistry, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	6	6	129
2	Engineering	3	3	71
3	Biochemistry	3	3	57
4	Biomolecular Engineering	2	2	41
5	Medicine	1	1	20

A. J. DUGGAN

Publications

245

Citations

H-Index

Page 1

	Year	Citations
Total synthesis of (.+-.)-pederamide Michael Adams, A. J. DUGGAN, Joel Smolanoff, Journal of the American Chemical Society Medicinal ChemistryMolecular SciencesChemical MeasurementChemical AnalysisDonut Icon	1979	48
Reaction of enolate anions with lactones A. J. DUGGAN, Michael Adams, Paul J. Brynes, Tetrahedron Letters Organic ChemistryChemistryEnolate AnionsAsymmetric CatalysisEnantioselective Synthesis	1978	41
Relative reactivity of substituted 2-alkoxy- and 2-phenoxy-3,4-dihydro-2H-pyrans with tert-butyl hypochlorite. Effect of substituents on reactivity and products Stan S. Hall, Guiseppe F. Weber, A. J. DUGGAN The Journal of Organic Chemistry Chemical EngineeringDerivative (Chemistry)EngineeringRelative ReactivityChemical Derivative	1978	30
Synthesis of δ‐Lactones from Glutaraldehyde M. Rosenberger, David W. Andrews, F. DiMaria, Helvetica Chimica Acta BiosynthesisBioorganic ChemistryDerivativesBiochemistryEngineering	1972	25
Phase-Transfer Mediated Heteroaromatic Nucleophilic Substitution: Introduction of a β-Adrenergic Blocking Moiety A. J. DUGGAN, Edward J. J. Grabowski, Warren K. Russ Synthesis β-Adrenergic Blocking MoietyMolecular PharmacologyBiochemistryMedicineBioconjugation	1980	20
Steroid Total Synthesis, Part VIII; (+)‐estr‐4‐ene‐3,17‐dione M. Rosenberger, A. J. DUGGAN, R. Borer, Helvetica Chimica Acta Mannich BaseEngineeringNatural SciencesDiversity-oriented SynthesisSteroid Total Synthesis	1972	16
Chemistry of 2-alkoxy-3,4-dihydro-2H-pyrans. IV. 3-Alkoxy-2-oxanorcaranes. Synthesis of labile cyclopropanes from labile olefins using an improved lithium-ammonia reduction procedure on the dichlorocarbene adducts A. J. DUGGAN, Stan S. Hall The Journal of Organic Chemistry HeterocyclicLabile CyclopropanesDichlorocarbene AdductsAltmetric Attention ScoreOrganic Chemistry	1975	14
Chemistry of 2-alkoxy-3,4-dihydro-2H-pyrans. III. Synthesis and solvolysis of the dichlorocarbene adducts 3-alkoxy-2-oxa-7,7-dichloronorcaranes A. J. DUGGAN, Stan S. Hall The Journal of Organic Chemistry Bioorganic ChemistryHeterocyclicNatural SciencesAltmetric Attention ScoreOrganic Chemistry	1975	14
The chemistry of 2-alkoxy-3,4-dihydro-2H-pyrans. 5. Addition of tert-butyl hypohalites to 3,4-dihydro-2H-pyran and its 2-alkoxy and 2-alkoxy-6-methyl derivatives in hydroxylic solvents A. J. DUGGAN, Stan S. Hall The Journal of Organic Chemistry Derivative (Chemistry)Bioorganic ChemistryDonut Icon2-Alkoxy-6-methyl DerivativesNatural Sciences	1977	14
Steroid Total Synthesis, Part VII; (±)‐estr‐4‐ene‐3, 17‐dione and (±) 13β‐ethyl‐gon‐4‐ene‐3, 17‐dione M. Rosenberger, A. J. DUGGAN, G. Saucy Helvetica Chimica Acta Practical SynthesisEarlier ResultsBiochemistryNatural SciencesPart Vii	1972	12

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