Steven J. Wittenberger

Author

Also Known As

S. J. WITTENBERGER, S. J. Wittenberger, S. WITTENBERGER, S.J. Wittenberger, Steven J. Wittenberger, Steven Wittenberger, Wittenberger, S.J.

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Abbott (United States)Abbott Fund Abbott (United Kingdom)AbbVie (United States)

About

Steven J. Wittenberger is an author at Abbott (United States) specializing in pharmacology, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	311
2	Natural Sciences	11	11	527
3	Biochemistry	11	12	577
4	Engineering	9	9	833
5	Law	1	1	30

Steven J. Wittenberger

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Dialkyltin oxide mediated addition of trimethylsilyl azide to nitriles. A novel preparation of 5-substituted tetrazols Steven J. Wittenberger, B. G. DONNER The Journal of Organic Chemistry Combinatorial ChemistryTrimethylsilyl AzideHeterocyclicAltmetric Attention Score5-Substituted Tetrazols	1993	269
Development of a Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes for the Synthesis of Endothelin-A Antagonist <b>ABT-546</b>. Scope, Mechanism, and Further Application to the Synthesis of the Antidepressant Rolipram David M. Barnes, Jianguo Ji, Michael G. Fickes, Journal of the American Chemical Society Asymmetric CatalysisMedicinal Chemistry1,3-Dicarbonyl CompoundsFurther ApplicationBiochemistry	2002	209
A Laser Driven Flow Chemistry Platform for Scaling Photochemical Reactions with Visible Light Kaid C. Harper, Eric G. Moschetta, Shailendra Bordawekar, ACS Central Science Laser Cstr PlatformVisible LightEngineeringSynthetic PhotochemistryChemistry	2019	180
Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes Jianguo Ji, David M. Barnes, Ji Zhang, Journal of the American Chemical Society 1,3-Dicarbonyl CompoundsEngineeringHeterocyclicAlkene MetathesisConjugate Acid-base Pairs	1999	151
2,2,2-Trifluoroethyl Formate: A Versatile and Selective Reagent for the Formylation of Alcohols, Amines, and<i>N</i>-Hydroxylamines David R. Hill, C.‐N. HSIAO, Ravi Kurukulasuriya, Organic Letters High Yields2,2,2-Trifluoroethyl FormateDerivative (Chemistry)EngineeringSelective Reagent	2001	98
Addition of Organometallic Reagents to N-Glycosyl Nitrones. Enantioselective Syntheses of (+)-(R)- and (-)-(S)-Zileuton Anwer Basha, Rodger F. Henry, Maureen A. McLaughlin, The Journal of Organic Chemistry EngineeringBiochemistryNatural SciencesAltmetric Attention ScoreOrganometallic Reagents	1994	52
A Scaleable Synthesis of Fiduxosin Anthony R. Haight, Anne E. Bailey, William S. Baker, Organic Process Research & Development O-aryl LactonePharmaceutical ScienceBioorganic ChemistryEngineeringOrganic Chemistry	2004	50
A sulfur-mediated total synthesis of Zygosporin E Edwin Vedējs, James D. Rodgers, Steven J. Wittenberger Journal of the American Chemical Society Molecular SciencesBiosynthesisBioorganic ChemistryBiochemistryEngineering	1988	43
Synthesis of cytochalasins: the route to sulfur-bridged [11]cytochalasans Edwin Vedējs, J. G. REID, James D. Rodgers, Journal of the American Chemical Society Molecular SciencesBioorganic ChemistryHeterocyclicBiochemistryDonut Icon	1990	40
Discovery of 2-[4-{{2-(2<i>S</i>,5<i>R</i>)-2-Cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]- 4-methyl-1-piperidinyl]-4-pyridinecarboxylic Acid (ABT-279): A Very Potent, Selective, Effective, and Well-Tolerated Inhibitor of Dipeptidyl Peptidase-IV, Useful for the Treatment of Diabetes David J. Madar, Hana Kopecka, Daisy Pireh, Journal of Medicinal Chemistry	2006	37

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