Bradley Brown - Concepedia

Author

Bradley Brown

Also Known As

B B BROWN, B. B. BROWN, B. B. Brown, B.B. Brown, Bradley B. Brown, Bradley Brown, Brown, Bradley, Christine Brown, Mihai Bce, Nicholas Steel

Publications

Citations

H-Index

Concepts

All Affiliations

Indiana University Bloomington Massachusetts Institute of Technology University of California, Berkeley

About

Bradley Brown is an author at Indiana University Bloomington specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	9	9	524
2	Natural Sciences	4	4	241
3	Medicine	3	3	65
4	Health Sciences	1	1	17
5	Nursing	1	1	17

Bradley Brown

Publications

960

Citations

H-Index

Page 1

	Year	Citations
Stereoselective synthesis of (Z,E)-2-bromo-1,3-dienes via the palladium (O) catalyzed cross coupling reactions of 1,1-dibromoolefins and vinylboronic acids William Roush, K.J.M. Moriarty, Bradley Brown Tetrahedron Letters Cross-coupling ReactionAlkene MetathesisVinylboronic AcidsOrganic ChemistryOrganometallic Catalysis	1990	110
Enantioselective synthesis of 2-alkyl-5-methylene-1,3-dioxolan-4-ones and exo-selective Diels-Alder reactions with cyclopentadiene William Roush, Bradley Brown The Journal of Organic Chemistry Asymmetric CatalysisHeterocyclicAlkene MetathesisNatural SciencesDiversity-oriented Synthesis	1992	97
A single-bead decode strategy using electrospray ionization mass spectrometry and a new photolabile linker: 3-Amino-3-(2-nitrophenyl)propionic acid Bradley Brown, David S. Wagner, H. Mario Geysen Molecular Diversity EngineeringAnalytical InstrumentationPhotochemistryBiochemistryNew Photolabile Linker	1995	96
The Per Case and Total Annual Costs of Foodborne Illness in the United States Travis Minor, Angela Lasher, Karl C. Klontz, Risk Analysis	2015	91
Enantioselective synthesis of the bottom half of chlorothricolide. 3. Studies of the steric directing group strategy for stereocontrol in intramolecular Diels-Alder reactions William Roush, Masanori Kageyama, Renata Riva, The Journal of Organic Chemistry HalogenationEngineeringAltmetric Attention ScoreOrganic ChemistrySocial Media Presence	1991	73
Application of the steric directing group strategy to the stereoselective synthesis of the octahydronaphthalene substructure of kijanolide and tetronolide William Roush, Bradley Brown Journal of the American Chemical Society Chemical EngineeringEngineeringDonut IconAltmetric Attention ScoreOrganic Chemistry	1993	72
A Formal Total Synthesis of (+)-Tetronolide, the Aglycon of the Tetrocarcins: Enantio- and Diastereoselective Syntheses of the Octahydronaphthalene (Bottom-Half) and Spirotetronate (Top-Half) Fragments William Roush, Melissa L. Reilly, Kazuo Koyama, The Journal of Organic Chemistry EngineeringOrganic ChemistryFormal Total SynthesisChemistryHeterocycle Chemistry	1997	72
A highly diastereo- and enantioselective synthesis of the top half of kijanolide William Roush, Bradley Brown The Journal of Organic Chemistry EngineeringAltmetric Attention ScoreBibliometricsOrganic ChemistryChemistry	1993	62
A highly stereoselective synthesis of the octahydronaphthalene subunit of kijanolide and tetronolide William Roush, Bradley Brown, Susan E. Drozda Tetrahedron Letters EngineeringOrganic ChemistryOctahydronaphthalene SubunitStereoselective SynthesisChemistry	1988	50
Synthesis and Diels-Alder reactions of 2-alkyl-5-methylene-1,3-dioxolan-4-ones and 2-alkyl-3-acyl-5-methylene-1,3-oxazolidin-4-ones: Highly exo and diastereoface selective chiral ketene equivalents William Roush, A. P. ESSENFELD, Joseph S. Warmus, Tetrahedron Letters EngineeringHeterocyclicDiels-alder ReactionsHighly ExoOrganic Chemistry	1989	49

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