What is she best known for?
The fields of study she is best known for:
- Organic chemistry
- Catalysis
- Alkene
Carmen Nájera mainly investigates Organic chemistry, Catalysis, Enantioselective synthesis, Aryl and Palladium.
All of her Organic chemistry and Heck reaction, Michael reaction, Benzoic acid, Methylamine and Nucleophile investigations are sub-components of the entire Organic chemistry study.
Her research integrates issues of Base, Polymer chemistry and Aqueous solution in her study of Catalysis.
Her research in Enantioselective synthesis intersects with topics in Amino acid, Aldol reaction, Cycloaddition and Stereochemistry.
Her Aryl research is multidisciplinary, relying on both Oxime, Medicinal chemistry, Homogeneous catalysis, Bromide and Sodium hydroxide.
Carmen Nájera combines subjects such as Conjugated system and Organic synthesis with her study of Palladium.
Her most cited work include:
- The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry† (2071 citations)
- Recent advances in Sonogashira reactions (941 citations)
- Organocatalytic asymmetric conjugate additions (710 citations)
What are the main themes of her work throughout her whole career to date?
Her primary scientific interests are in Organic chemistry, Catalysis, Enantioselective synthesis, Medicinal chemistry and Stereochemistry.
Her work in Aldol reaction, Reagent, Electrophile, Aqueous solution and Alkyl are all subfields of Organic chemistry research.
Her work deals with themes such as Aryl, Oxime and Polymer chemistry, which intersect with Catalysis.
Her Aryl study frequently links to related topics such as Sonogashira coupling.
As part of one scientific family, Carmen Nájera deals mainly with the area of Enantioselective synthesis, narrowing it down to issues related to the Amino acid, and often Hydrolysis.
The Medicinal chemistry study combines topics in areas such as Yield, Sulfone, Allylic rearrangement, Nucleophile and Stereoselectivity.
She most often published in these fields:
- Organic chemistry (53.47%)
- Catalysis (36.53%)
- Enantioselective synthesis (28.06%)
What were the highlights of her more recent work (between 2013-2021)?
- Catalysis (36.53%)
- Organic chemistry (53.47%)
- Medicinal chemistry (26.25%)
In recent papers she was focusing on the following fields of study:
Her primary areas of investigation include Catalysis, Organic chemistry, Medicinal chemistry, Enantioselective synthesis and Palladium.
Her Catalysis study incorporates themes from Aryl, Oxime, Polymer chemistry and Copper.
Her Organocatalysis, Aldol reaction, Cycloaddition, Aqueous solution and Michael reaction investigations are all subjects of Organic chemistry research.
In Medicinal chemistry, Carmen Nájera works on issues like Group, which are connected to Decomposition and Tetrazole.
Her Enantioselective synthesis study combines topics in areas such as Electrophile and Tosyl, Stereochemistry.
Her Palladium study integrates concerns from other disciplines, such as Inorganic chemistry, Nanoparticle, Ligand and Heterogeneous catalysis.
Between 2013 and 2021, her most popular works were:
- Chemicals from Alkynes with Palladium Catalysts (469 citations)
- 1,3-Dipolar cycloadditions of azomethine imines (125 citations)
- Catalytic asymmetric transfer hydrogenation of ketones: recent advances (124 citations)
In her most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Catalysis, Organic chemistry, Palladium, Enantioselective synthesis and Aryl are her primary areas of study.
Specifically, her work in Catalysis is concerned with the study of Sonogashira coupling.
Her work carried out in the field of Organic chemistry brings together such families of science as Medicinal chemistry and Polymer chemistry.
Her Enantioselective synthesis research includes themes of Group 2 organometallic chemistry, Stereochemistry and Enamine.
Carmen Nájera interconnects Adduct and Stereoselectivity in the investigation of issues within Stereochemistry.
The concepts of her Aryl study are interwoven with issues in Coupling reaction and Magnesium.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
