What is she best known for?
The fields of study she is best known for:
- Organic chemistry
- Catalysis
- Biochemistry
Her primary scientific interests are in Stereochemistry, Organic chemistry, Total synthesis, Combinatorial chemistry and Reagent.
Her Stereochemistry study combines topics in areas such as Ether and Biological activity.
Her studies deal with areas such as Amino acid and Ninhydrin as well as Organic chemistry.
The concepts of her Total synthesis study are interwoven with issues in Moiety and Nucleophilic aromatic substitution.
Her Combinatorial chemistry study combines topics from a wide range of disciplines, such as Scientific method, Sulfur, Camphorsultam, Michael reaction and Oxygen.
Her work carried out in the field of Reagent brings together such families of science as Dipeptide, Racemization and Coupling reagent.
Her most cited work include:
- Control of angiogenesis with synthetic heparin substitutes (289 citations)
- Ninhydrin and ninhydrin analogs. Syntheses and applications (132 citations)
- Natural products as probes of cell biology: 20 years of didemnin research. (118 citations)
What are the main themes of her work throughout her whole career to date?
Madeleine M. Joullié mainly focuses on Stereochemistry, Organic chemistry, Total synthesis, Amino acid and Combinatorial chemistry.
Her Stereochemistry study combines topics in areas such as Ring and Stereoselectivity.
Madeleine M. Joullié mostly deals with Reagent in her studies of Organic chemistry.
Total synthesis and Ether are commonly linked in her work.
Her Depsipeptide research focuses on Cyclic peptide and how it relates to Chemical synthesis.
The various areas that Madeleine M. Joullié examines in her Didemnin B study include Biological activity and Didemnin.
She most often published in these fields:
- Stereochemistry (38.76%)
- Organic chemistry (34.63%)
- Total synthesis (14.99%)
What were the highlights of her more recent work (between 2004-2021)?
- Stereochemistry (38.76%)
- Total synthesis (14.99%)
- Organic chemistry (34.63%)
In recent papers she was focusing on the following fields of study:
Madeleine M. Joullié spends much of her time researching Stereochemistry, Total synthesis, Organic chemistry, Ring and Stereoselectivity.
Madeleine M. Joullié works on Stereochemistry which deals in particular with Moiety.
Her Total synthesis research is multidisciplinary, incorporating perspectives in Tubulin, Phenylahistin, Fermentation and Organic synthesis.
Her Ring research includes themes of Carbon, Catalysis, Enantioselective synthesis and Formic acid.
Her Stereoselectivity study integrates concerns from other disciplines, such as Intramolecular force and Aziridine.
In her study, Combinatorial chemistry is strongly linked to Ninhydrin, which falls under the umbrella field of Reagent.
Between 2004 and 2021, her most popular works were:
- The development of novel ninhydrin analogues. (102 citations)
- Evolution of amide bond formation (82 citations)
- A central strategy for converting natural products into fluorescent probes. (74 citations)
In her most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Biochemistry
Stereochemistry, Organic chemistry, Stereoselectivity, Total synthesis and Aziridine are her primary areas of study.
Her Stereochemistry research incorporates elements of Biological activity, Chemical synthesis and Ring.
Her Organic chemistry research is multidisciplinary, relying on both Ninhydrin and Forensic chemistry.
Her Total synthesis research integrates issues from Tubulin, Plasma protein binding and Molecular model.
Madeleine M. Joullié interconnects Ether, Phenol, Ustiloxin D, Longest linear sequence and Alkyl in the investigation of issues within Aziridine.
In her research, Didemnin, Didemnin B and Structure–activity relationship is intimately related to Natural product, which falls under the overarching field of Depsipeptide.
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