What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His scientific interests lie mostly in Organic chemistry, Combinatorial chemistry, Medicinal chemistry, Stereochemistry and Cyclopropane.
His work is connected to Nucleophile, Stereoselectivity, Organic synthesis, Electrophile and Catalysis, as a part of Organic chemistry.
His work deals with themes such as Derivative, Supramolecular chemistry and Samarium, which intersect with Combinatorial chemistry.
His Medicinal chemistry study integrates concerns from other disciplines, such as Alkylation, Samarium diiodide, Nitrile, Indole test and Ion.
Hans-Ulrich Reissig interconnects Bond cleavage, Oxazines and Enantiopure drug, Enantioselective synthesis in the investigation of issues within Stereochemistry.
His research in Cyclopropane intersects with topics in Transition metal carbene complex, Carbene and Sigmatropic reaction.
His most cited work include:
- Donor-acceptor-substituted cyclopropane derivatives and their application in organic synthesis. (927 citations)
- Sugars, Alkaloids, and Heteroaromatics: Exploring Heterocyclic Chemistry with Alkoxyallenes† (264 citations)
- Nine Times Fluoride can be Good for your Syntheses. Not just Cheaper: Nonafluorobutanesulfonates as Intermediates for Transition Metal-Catalyzed Reactions (96 citations)
What are the main themes of his work throughout his whole career to date?
Hans-Ulrich Reissig spends much of his time researching Organic chemistry, Medicinal chemistry, Stereochemistry, Combinatorial chemistry and Enantiopure drug.
Oxazines, Enol, Pyridine, Stereoselectivity and Catalysis are among the areas of Organic chemistry where the researcher is concentrating his efforts.
His research in Catalysis is mostly focused on Palladium.
His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Samarium, Samarium diiodide, Ring, Alkoxy group and Intramolecular force.
Hans-Ulrich Reissig has researched Samarium in several fields, including Indole test and Ketyl.
Many of his studies involve connections with topics such as Bicyclic molecule and Enantiopure drug.
He most often published in these fields:
- Organic chemistry (42.88%)
- Medicinal chemistry (26.92%)
- Stereochemistry (17.53%)
What were the highlights of his more recent work (between 2014-2021)?
- Organic chemistry (42.88%)
- Medicinal chemistry (26.92%)
- Combinatorial chemistry (16.74%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Organic chemistry, Medicinal chemistry, Combinatorial chemistry, Stereochemistry and Regioselectivity.
His study in Organic chemistry concentrates on Enantiopure drug, Pyridine, Allene, Moiety and Diels alder.
His Medicinal chemistry research includes elements of Samarium, Alkoxy group, Crystal structure and Catalysis.
His Combinatorial chemistry research includes themes of Natural product, Sodium azide, Corrole, Nucleophile and Nucleophilic substitution.
His studies in Stereochemistry integrate themes in fields like Stereocenter, Cycloaddition, Strain, Bipyridine and Cyclobutane.
His Regioselectivity study also includes fields such as
- Cascade reaction most often made with reference to Reductive amination,
- Indole test and related Yield.
Between 2014 and 2021, his most popular works were:
- The Huisgen Reaction: Milestones of the 1,3-Dipolar Cycloaddition. (45 citations)
- Nucleophilic Substitution on (Pentafluorophenyl)dipyrromethane: A New Route to Building Blocks for Functionalized BODIPYs and Tetrapyrroles (39 citations)
- Thrilling Strain! Donor–Acceptor‐Substituted Cyclobutanes for the Synthesis of (Hetero)Cyclic Compounds (28 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Hans-Ulrich Reissig focuses on Organic chemistry, Combinatorial chemistry, Stereochemistry, Pyridine and Cycloaddition.
Hans-Ulrich Reissig combines topics linked to Medicinal chemistry with his work on Organic chemistry.
He combines subjects such as BODIPY, Nucleophilic aromatic substitution, Nucleophilic substitution, Sodium azide and Nucleophile with his study of Combinatorial chemistry.
His studies deal with areas such as Stereocenter, Bipyridine, Homogeneous catalysis and Stereoselectivity as well as Stereochemistry.
His Pyridine study combines topics in areas such as Thiophene, Molecule, Ferrocene and Coupling reaction.
In the subject of general Cycloaddition, his work in Cyclobutanes is often linked to Donor acceptor, thereby combining diverse domains of study.
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