2009 - Fellow of the American Chemical Society
2005 - Fellow of the American Academy of Arts and Sciences
1998 - ACS Award for Encouraging Women into Careers in the Chemical Sciences, American Chemical Society (ACS)
1978 - Garvan–Olin Medal, American Chemical Society (ACS)
1957 - Fellow of the American Association for the Advancement of Science (AAAS)
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.
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.
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.
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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Control of angiogenesis with synthetic heparin substitutes
Judah Folkman;Paul B. Weisz;Madeleine M. Joullié;William W. Li.
Ninhydrin and ninhydrin analogs. Syntheses and applications
Madeleine M. Joullié;Tracy R. Thompson;Norman H. Nemeroff.
Natural products as probes of cell biology: 20 years of didemnin research.
Matthew D. Vera;Madeleine M. Joullié.
Medicinal Research Reviews (2002)
Evolution of amide bond formation
Madeleine M Joullie;Kenneth M Lassen.
The development of novel ninhydrin analogues.
Darren B. Hansen;Madeleine M. Joullié.
Chemical Society Reviews (2005)
Total synthesis of (+)-furanomycin and stereoisomers
J. Edward Semple;Pen C. Wang;Zenon Lysenko;Madeleine M. Joullie.
Journal of the American Chemical Society (1980)
Total synthesis and structural investigations of didemnins A, B, and C
Wen Ren Li;William R. Ewing;Bruce D. Harris;Madeleine M. Joullie.
Journal of the American Chemical Society (1990)
Phenylselenoetherification. A highly efficient cyclization process for the synthesis of oxygen- and sulfur-heterocycles
K. C. Nicolaou;R. L. Magolda;W. J. Sipio;W. E. Barnette.
Journal of the American Chemical Society (1980)
Mechanism of imidazole catalysis in the curing of epoxy resins
Fiore Ricciardi;William A. Romanchick;Madeleine M. Joullié.
Journal of Polymer Science Part A (1983)
Total synthesis of (-)-nummularine F
Robert J. Heffner;Jianjun Jiang;Madeleine M. Joullie.
Journal of the American Chemical Society (1992)
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