Jan Haller - Concepedia

Author

Jan Haller

University of California, Los Angeles

Also Known As

J. HALLER, J. Haller, Jan Haller

Publications

643

Citations

H-Index

Concepts

All Affiliations

University of California, Los Angeles University of Münster

About

Jan Haller is an author at University of California, Los Angeles specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	7	7	552
2	Natural Sciences	5	5	392
3	Biomolecular Engineering	4	4	162
4	Biochemistry	3	3	290
5	Medicine	1	1	59

Jan Haller

Publications

643

Citations

H-Index

Page 1

	Year	Citations
Experimental and Theoretical Kinetic Isotope Effects for Asymmetric Dihydroxylation. Evidence Supporting a Rate-Limiting “(3 + 2)” Cycloaddition Albert J. DelMonte, Jan Haller, K. N. Houk, Journal of the American Chemical Society EngineeringChemical TransformationBiochemistryCalifornia Los AngelesNatural Sciences	1997	249
Enantioselective synthesis via sparteine-induced asymmetric deprotonation D. HOPPE, Folker Hintze, Petra Tebben, Pure and Applied Chemistry EngineeringSparteine-induced Asymmetric DeprotonationOrganic ChemistryStereoselective SynthesisAsymmetric Catalysis	1994	101
Rationalizing the Stereoselectivity of Osmium Tetroxide Asymmetric Dihydroxylations with Transition State Modeling Using Quantum Mechanics-Guided Molecular Mechanics Per‐Ola Norrby, Torben Rasmussen, Jan Haller, Journal of the American Chemical Society Corey ModelsAsymmetric CatalysisEngineeringForce FieldPhysics	1999	82
Models for Stereoselective Additions to Chiral Allylic Ethers: Osmium Tetroxide Bis-hydroxylations Jan Haller, K. N. Houk Journal of the American Chemical Society	1997	68
Notification about the Explosive Properties of Togni’s Reagent II and One of Its Precursors Nikolaus Fiederling, Jan Haller, Heiko Schramm Organic Process Research & Development Molecular SciencesTogni ’EngineeringChemical AnalysisMedicine	2013	59
Kinetic Resolution of β-Stereogenic<i>O</i>-Alkyl Carbamates by (-)-Sparteine-Assisted Deprotonation. External versus Internal Chiral Induction. Jan Haller, Thomas Hense, Dieter Hoppe Synlett Methyl CarbamateEngineeringBiochemistryInternal Chiral InductionKinetic Resolution	1993	25
Stereoselective Diels−Alder Reactions of Hexachlorocyclopentadiene with Chiral Alkenes: New Insights Into the “Inside-Alkoxy” Model of Stereoselectivity Jan Haller, Satomi Niwayama, How-Yunn Duh, The Journal of Organic Chemistry	1997	23
Why Is the Concerted (2+2) Mechanism of the Reactions of SO<sub>3</sub> with Alkenes Favored over the (3+2) Mechanism? Density Functional and Correlated ab Initio Calculations and a Frontier MO Analysis Jan Haller, Brett R. Beno, K. N. Houk Journal of the American Chemical Society EngineeringMp2 CalculationsOrganic ChemistryComputational ChemistryChemistry	1998	20
Experimental and Theoretical Studies of the Internal Stereodifferentiation Occurring During the Lithiation of β‐Stereogenic Alkyl Carbamates. Kinetic Resolutions by (‐)‐Sparteine‐Mediated Deprotonation Jan Haller, Thomas Hense, Dieter Hoppe Liebigs Annalen Transition StatesInternal Stereodifferentiation OccurringEngineeringBiochemistryKinetic Resolution	1996	16

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