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Carbocycloaddition Strategies for Troponoid Synthesis.
Murelli, Ryan P; Berkowitz, Alex J; Zuschlag, Daniel W.
Afiliación
  • Murelli RP; Department of Chemistry, Brooklyn College, The City University of New York, Brooklyn, NY, 11210, United States.
  • Berkowitz AJ; Ph.D. Program in Chemistry, The Graduate Center of the City University of New York, New York, NY, 10016, United States.
  • Zuschlag DW; Ph.D. Program in Biochemistry, The Graduate Center of the City University of New York, New York, NY, 10016, United States.
Tetrahedron ; 1302023 Jan 09.
Article en En | MEDLINE | ID: mdl-36777111
Tropone is the prototypical aromatic 7-membered ring, and can be found in virtually any undergraduate textbook as a key example of non-benzenoid aromaticity. Aside from this important historical role, tropone is also of high interest as a uniquely reactive synthon in complex chemical synthesis as well as a valuable chemotype in drug design. More recently, there has been growing interest in the utility of tropones for catalysis and material science. Thus, synthetic strategies capable of synthesizing functional tropones are key to fully exploiting the potential of this aromatic ring system. Cycloaddition reactions are particularly powerful methods for constructing carbocycles, and these strategies in turn have proven to be powerful for generating troponoids. The following review article provides an overview of strategies for troponoids wherein the 7-membered carbocycle is generated through a cycloaddition reaction. Representative examples of each strategy are also provided.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Tetrahedron Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Tetrahedron Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos