Michael Widhalm - Catalysis

Author Information

Michael Widhalm is affiliated with the Institute of Chemical Catalysis at the University of Vienna, located at Währinger Straße 38, 1090 Wien, Austria. His research primarily focuses on the synthesis and characterization of chiral compounds, particularly those involving ferrocene derivatives and novel organocatalysts.

Research Contributions

Michael Widhalm has made significant contributions to the field of chemical catalysis, with a particular emphasis on the synthesis and characterization of enantiopure and planar-chiral compounds. His work frequently involves the use of chiral ammonium salt catalysis and the development of new methods for producing orthogonally functionalized compounds with quaternary stereocenters. Widhalm has also explored the structural and reactive properties of various phosphorus-linked ferrocenes and dinaphthoazepinium salts, contributing valuable insights into their potential applications in catalysis and material science.

Aliases

Michael Widhalm publishes under several aliases, including M Widhalm, M. Widhalm, and Michael Widhalm.

Publication and Citation Metrics

Metric	Value
Citation Count	1582
h-index	22
Paper Count	114

Publications:

Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes

DOI: 10.1107/S2053229621001996

Year: 2021

Racemic and Meso Crystal Structures of an Axial-Chiral Spirobi-(dinaphthoazepin)ium Salt: Emergence of an S4-Symmetric Molecule

DOI: 10.3390/sym13081365

Year: 2021

Enantioselective Synthesis of Acyclic Orthogonally Functionalized Compounds Bearing a Quaternary Stereocenter Using Chiral Ammonium Salt Catalysis

DOI: 10.1002/open.202100162

Year: 2021

(2Sp,4R,8Sp)-4-Methyl-1-phenyl-diferroceno-5-Z-ethylene-1-phosphinoxide

DOI: 10.3390/m1105

Year: 2020

Planar-Chiral P and N-bridged Diferrocenes

DOI: 10.3390/m1130

Year: 2020

molbank Communication ( 2 S p , 4 R , 6 R , 8 S p )-4 , 6-Dimethyl-1-phenyl-diferroceno-1-phosphines

DOI:

Year: 2019

Synthesis, Structure, and Reactivity of Binaphthyl Supported Dihydro[1,6]diazecines

DOI: 10.3390/molecules24173098

Year: 2019

(2Sp,4R,6R,8Sp)-4,6-Dimethyl-1-phenyl-diferroceno-1-phosphines

DOI: 10.3390/m1098

Year: 2019

Formaldehyde-1,1″-(phenylphosphinidenesulfide)bis[(2S)-2-[(1R)-1-(methylamino)-ethyl]]ferrocene-aminal

DOI: 10.3390/m1090

Year: 2019

Improved Access to Chiral Tetranaphthoazepinium-Based Organocatalysts Using Aqueous Ammonia as Nitrogen Source

DOI: 10.3390/molecules24213844

Year: 2019

Why is Steady State Approximation Important?

What is Bromoethanesulfonate?

Why is Partial Oxidation Important?

What future trends could alleviate economic constraints in catalysis?

How Do Enzymes Function as Catalysts in ELISAs?

Why are Carbon Environments Important in Catalysis?

What Are the Key Metrics for Catalyst Standards?

What Types of Catalysts Can Be Synthesized Using FSP?

How to Handle Spills and Leaks?

How Can Understanding the Warburg Effect Lead to Better Cancer Treatments?

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