His scientific interests lie mostly in Stereochemistry, Total synthesis, Natural product, Biochemistry and Proteome. His Stereochemistry study which covers Ring that intersects with Stereoselectivity, Catalysis, Alkene and Palladium. In the field of Total synthesis, his study on Retrosynthetic analysis overlaps with subjects such as Degradation.
His Natural product research incorporates elements of Tubulin and Paclitaxel. His Paclitaxel research is multidisciplinary, incorporating perspectives in Taxadiene, Microtubule, Chemical synthesis and Semisynthesis. His study of Enzyme is a part of Biochemistry.
His primary areas of investigation include Stereochemistry, Organic chemistry, Combinatorial chemistry, Total synthesis and Natural product. His research on Stereochemistry also deals with topics like
Erik J. Sorensen specializes in Total synthesis, namely Retrosynthetic analysis. His work deals with themes such as Reactive intermediate and Chemical synthesis, which intersect with Natural product. Erik J. Sorensen studied Biochemistry and Tubulin that intersect with Paclitaxel, Taxus brevifolia and Semisynthesis.
Erik J. Sorensen spends much of his time researching Stereochemistry, Catalysis, Enzyme, Combinatorial chemistry and Cytochrome P450. The study incorporates disciplines such as Stereoisomerism, Ether, Ring, Chemical synthesis and Nucleophile in addition to Stereochemistry. Erik J. Sorensen interconnects Total synthesis, Dehydration, Polyketide and Epoxide in the investigation of issues within Stereoisomerism.
His Catalysis research is multidisciplinary, incorporating elements of Hydrogen atom abstraction, Nanotechnology and Medicinal chemistry. His Nanotechnology study incorporates themes from Natural product and Retrosynthetic analysis. His Enzyme research is included under the broader classification of Biochemistry.
His primary scientific interests are in Catalysis, Stereochemistry, Hydroxylation, Combinatorial chemistry and Reagent. His Catalysis research integrates issues from Photochemistry, Fluorine and Hydrogen atom abstraction. His Stereochemistry research is multidisciplinary, relying on both Stereoisomerism, Dehydration, Carbene, Site selective and Chemical synthesis.
His Hydroxylation study is associated with Biochemistry. His Combinatorial chemistry study combines topics in areas such as Yield, Organic chemistry, Anthranilic acid and Aryl. His Reagent research incorporates themes from Benzaldehyde, Medicinal chemistry, Ligand, Crystal structure and Alkyl.
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.
Classics in total synthesis : targets, strategies, methods
K. C. Nicolaou;E. J. Sorensen;E. J. Corey;Scott A. Snyder.
(1996)
Total synthesis of taxol
K. C. Nicolaou;K. C. Nicolaou;Z. Yang;J. J. Liu;H. Ueno.
Nature (1994)
Recent applications of C–H functionalization in complex natural product synthesis
Dylan J. Abrams;Philip A. Provencher;Erik J. Sorensen.
Chemical Society Reviews (2018)
Palladium-catalyzed ring-forming aminoacetoxylation of alkenes.
Erik J. Alexanian;Chulbom Lee;Erik J. Sorensen.
Journal of the American Chemical Society (2005)
Total Synthesis of (–)‐Epothilone A
Aaron Balog;Dongfang Meng;Ted Kamenecka;Peter Bertinato.
Angewandte Chemie (1996)
Total Synthesis of Taxol. 2. Construction of A and C Ring Intermediates and Initial Attempts To Construct the ABC Ring System
K. C. Nicolaou;J. J. Liu;Z. Yang;H. Ueno.
Journal of the American Chemical Society (1995)
Total Syntheses of Epothilones A and B
Dongfang Meng;Peter Bertinato;Aaron Balog;Dai Shi Su.
Journal of the American Chemical Society (1997)
Protein-reactive natural products.
Carmen Drahl;Benjamin F. Cravatt;Erik J. Sorensen.
Angewandte Chemie (2005)
Proteomic profiling of mechanistically distinct enzyme classes using a common chemotype.
Gregory C. Adam;Erik J. Sorensen;Benjamin F. Cravatt.
Nature Biotechnology (2002)
Total Synthesis of Taxol. 1. Retrosynthesis, Degradation, and Reconstitution
K. C. Nicolaou;P. G. Nantermet;H. Ueno;R. K. Guy.
Journal of the American Chemical Society (1995)
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