2011 - Fellow of the American Chemical Society
2007 - Fellow of the American Association for the Advancement of Science (AAAS)
1992 - Fellow of Alfred P. Sloan Foundation
Scott D. Rychnovsky mainly focuses on Stereochemistry, Organic chemistry, Prins reaction, Total synthesis and Enantioselective synthesis. His research links Polyene with Stereochemistry. His Prins reaction research is multidisciplinary, incorporating elements of Tetrahydropyran, Cope rearrangement, Oxocarbenium, Stereoisomerism and Solvolysis.
His Tetrahydropyran research integrates issues from Regioselectivity and Stereoselectivity. His research in Total synthesis tackles topics such as Enantiomer which are related to areas like Chain and Triketone. His Enantioselective synthesis study combines topics from a wide range of disciplines, such as Azide and Imide.
His primary scientific interests are in Organic chemistry, Stereochemistry, Combinatorial chemistry, Stereoselectivity and Reagent. His study in Organic chemistry focuses on Catalysis, Prins reaction, Acetal, Alkylation and Enantioselective synthesis. The study of Prins reaction is intertwined with the study of Cope rearrangement in a number of ways.
His Stereochemistry study integrates concerns from other disciplines, such as Tetrahydropyran, Ring and Polyene. Combinatorial chemistry is often connected to Mass spectrometry in his work. Scott D. Rychnovsky interconnects Alkene, Medicinal chemistry and Synthon in the investigation of issues within Stereoselectivity.
Scott D. Rychnovsky spends much of his time researching Combinatorial chemistry, Organic chemistry, Stereochemistry, Mass spectrometry and Absolute configuration. His Combinatorial chemistry research is multidisciplinary, relying on both Coupling reaction, Halide, Aryl and Peptide. Scott D. Rychnovsky performs multidisciplinary study on Organic chemistry and Acetylation in his works.
Specifically, his work in Stereochemistry is concerned with the study of Intramolecular force. His study in Mass spectrometry is interdisciplinary in nature, drawing from both Sulfoxide, Computational biology, Cross-Linking Reagents and Protein–protein interaction. His studies deal with areas such as Kinetic resolution, Catalysis, Enantioselective synthesis, Acylation and 1h nmr spectroscopy as well as Absolute configuration.
Scott D. Rychnovsky mainly investigates Protein–protein interaction, Biochemistry, Organic chemistry, Mass spectrometry and Ring. The Protein–protein interaction study combines topics in areas such as Amino acid, Plasma protein binding, Lipid metabolism and Proteasome. The concepts of his Mass spectrometry study are interwoven with issues in Combinatorial chemistry, Computational biology and Cross-Linking Reagents.
His study in Ring is interdisciplinary in nature, drawing from both Alkylation, Total synthesis and Synthon. Total synthesis is a subfield of Stereochemistry that Scott D. Rychnovsky investigates. His Stereochemistry research includes elements of Silyl enol ether, Diels alder and Regioselectivity.
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Stereochemistry of alternating polyol chains: 13C NMR analysis of 1,3-diol acetonides
Scott D. Rychnovsky;Donald J. Skalitzky.
Tetrahedron Letters (1990)
Analysis of two carbon-13 NMR correlations for determining the stereochemistry of 1,3-diol acetonides
Scott D. Rychnovsky;Bruce Rogers;Guang Yang.
Journal of Organic Chemistry (1993)
Oxo Polyene Macrolide Antibiotics
Scott D. Rychnovsky.
Chemical Reviews (1995)
Configurational Assignment of Polyene Macrolide Antibiotics Using the [13C]Acetonide Analysis
Scott D. Rychnovsky;and Bruce N. Rogers;Timothy I. Richardson.
Accounts of Chemical Research (1998)
Development of a Novel Cross-linking Strategy for Fast and Accurate Identification of Cross-linked Peptides of Protein Complexes
Athit Kao;Chi-li Chiu;Danielle Vellucci;Yingying Yang.
Molecular & Cellular Proteomics (2011)
Free-radical cyclization of bromo acetals. Use in the construction of bicyclic acetals and lactones
Gilbert Stork;Robert Mook;Scott A. Biller;Scott D. Rychnovsky.
Stereocontrolled synthesis of cis-2,5-disubstituted tetrahydrofurans and cis- and trans-linalyl oxides
Scott D. Rychnovsky;Paul A. Bartlett.
Journal of the American Chemical Society (1981)
Predicting NMR spectra by computational methods: structure revision of hexacyclinol.
Scott D. Rychnovsky.
Organic Letters (2006)
Mukaiyama aldol-Prins cyclization cascade reaction: a formal total synthesis of leucascandrolide A.
David J. Kopecky;Scott D. Rychnovsky.
Journal of the American Chemical Society (2001)
Synthesis of (-)-centrolobine by Prins cyclizations that avoid racemization.
Shinji Marumoto;James J Jaber;Justin P Vitale;Scott D Rychnovsky.
Organic Letters (2002)
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