David Brown - Concepedia

Concepedia

Author

David Brown

Pfizer (United Kingdom)ORCID

Also Known As

D. BROWN, D. Brown, D.M.L. Brown, David Brown, David M. Brown, David M. L. Brown

22

Publications

1.8K

Citations

9

H-Index

38

Concepts

All Affiliations

Pfizer (United Kingdom)University of Oxford Pacific Northwest National Laboratory

DB

About

David Brown is an author at Pfizer (United Kingdom) specializing in natural sciences, engineering, and biomolecular engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	5	5	111
2	Natural Sciences	5	5	127
3	Biochemistry	4	4	106
4	Medicine	1	1	27
5	Social Sciences	1	1	27

David Brown

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9

Publications

1.8K

Citations

9

H-Index

	Year	Citations
Dominant and diet-responsive groups of bacteria within the human colonic microbiota Alan W. Walker, Jennifer Ince, Sylvia H. Duncan, The ISME Journal	2010	1.6K
The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans Sik-man S. Choi, Paul M. Myerscough, Antony J. Fairbanks, Journal of the Chemical Society Chemical Communications Group α-SubstituentsEngineeringBiochemistryFunctionalised Homochiral TetrahydrofuransExcellent Yield	1992	37
3-Hydroxymuscarines from L-Rhamnose Simon J. Mantell, Peter S. Ford, David J. Watkin, Tetrahedron Medicinal ChemistryBioorganic ChemistryBiochemistryNatural SciencesStereoselective Synthesis	1993	36
Deep Learning-Enabled MS/MS Spectrum Prediction Facilitates Automated Identification Of Novel Psychoactive Substances Fei Wang, Daniel Pasin, Michael A. Skinnider, Analytical Chemistry Hit IdentificationPsychopharmacologyForensic ChemistrySocial SciencesTandem Mass Spectrometry	2023	27
A practical synthesis of (+)-muscarine from L-rhamnose Simon J. Mantell, George W. J. Fleet, David Brown Journal of the Chemical Society Perkin Transactions 1 Practical SynthesisBioorganic ChemistryEngineeringNatural SciencesDiversity-oriented Synthesis	1992	21
Acid-catalysed transformation of α-trifluoromethanesulfonates of γ- and δ-lactones into 2,5-disubstituted homochiral tetrahydrofurans Joseph R. Wheatley, C. J. F. BICHARD, Simon J. Mantell, Journal of the Chemical Society Chemical Communications 2,5-Disubstituted Homochiral TetrahydrofuransMethanolic SolutionMethyl Tetrahydrofuran-α-carboxylatesEngineeringMethanol	1993	21
3R-Hydroxymuscarine from L-rhamnose without protection Simon J. Mantell, Peter S. Ford, David J. Watkin, Tetrahedron Letters Medicinal ChemistryPharmaceutical ScienceBiochemistryNatural SciencesHerbal Medicine	1992	17
Kinetic and thermodynamic azides from α-triflates of γ-lactones: intermediates for the incorporation of polyhydroxylated<scp>D</scp>- and<scp>L</scp>-α-aminoacids into combinatorial libraries Thomas M. Krülle, Benjamin G. Davis, Helen Ardron, Chemical Communications Combinatorial ChemistryEnantioselective SynthesisEngineeringBiochemistryCombinatorial Libraries	1996	16
Transparent system-level migration of PGAS applications using Xen on InfiniBand Daniele Paolo Scarpazza, P. Mullaney, Oreste Villa, Cluster ComputingEngineeringComputer ArchitectureFault ToleranceFault-tolerant Messaging	2007	16

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