Franz J. Weiberth - Concepedia

Author

Franz J. Weiberth

Sanofi (United States)ORCID

Also Known As

F. J. WEIBERTH, Franz J. Weiberth, Franz Weiberth

Publications

889

Citations

H-Index

Concepts

All Affiliations

Sanofi (United States)

About

Franz J. Weiberth is an author at Sanofi (United States) specializing in organic chemistry, pharmacology, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	5	5	803
2	Natural Sciences	5	5	684
3	Biochemistry	3	3	61
4	Biomolecular Engineering	3	3	67
5	Medicine	2	2	51

Franz J. Weiberth

Publications

864

Citations

H-Index

Page 1

	Year	Citations
Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited Marian C. Bryan, Peter J. Dunn, David A. Entwistle, Green Chemistry EngineeringChemical TransformationGreen ChemistryGreenness AssessmentOrganic Chemistry	2018	582
Copper(I)-activated addition of Grignard reagents to nitriles. Synthesis of ketimines, ketones, and amines Franz J. Weiberth, Stan S. Hall The Journal of Organic Chemistry Chemical EngineeringEngineeringChemical AnalysisGrignard ReagentsAltmetric Attention Score	1987	113
Alkylation-reduction of carbonyl systems. Part 14. Tandem alkylation-reduction. Highly stereoselective synthesis of (E)-1-hydroxymethyl methyl propenyl ethers from aldehydes using 1-lithio-1-methoxyallene Franz J. Weiberth, Stan S. Hall The Journal of Organic Chemistry Highly Stereoselective SynthesisChemical EngineeringEngineeringDonut IconMethyl Propenyl Ethers	1985	42
Demonstration on Pilot-Plant Scale of the Utility of 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) as a Catalyst in the Efficient Amidation of an Unactivated Methyl Ester Franz J. Weiberth, Yong Yu, Witold Subotkowski, Organic Process Research & Development Bioorganic ChemistryEngineeringH-pgds InhibitorOrganic ChemistryChemistry	2012	41
Chemical Development of MDL 103371: An <i>N</i>-Methyl-<scp>d</scp>-Aspartate-Type Glycine Receptor Antagonist for the Treatment of Stroke Timothy Watson, Stephen W. Horgan, Ramnik S. Shah, Organic Process Research & Development Pharmaceutical ScienceChemical DevelopmentMdl 103371PharmacotherapyChemical Biology	2000	35
Tandem alkylation-reduction of nitriles. Synthesis of branched primary amines Franz J. Weiberth, Stan S. Hall The Journal of Organic Chemistry EngineeringChemical AnalysisTandem Alkylation-reductionAltmetric Attention ScoreChemometrics	1986	25
Process Development of Selectively Benzoylated and Fluorinated Glycosyl Donors Franz J. Weiberth, Harpal S. Gill, Ying Jiang, Organic Process Research & Development Combinatorial ChemistryRoute SelectionGlycobiologyOrganic ChemistryPharmaceutical Chemistry	2010	16
“One-pot” preparation of N-(Carbonylamino)amino acids and half-acid/half-ester urea dipeptides directly from α-amio acids Franz J. Weiberth Tetrahedron Letters Bioorganic ChemistryAmino AcidsBiochemistryNatural Sciencesα-Amio Acids	1999	10

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