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Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances

期刊

MOLECULES
卷 20, 期 9, 页码 16103-16126

出版社

MDPI
DOI: 10.3390/molecules200916103

关键词

cycloaddition reactions; BINOL-derived phosphoric acids; N-triflyl phosphoramides; enantioselective pericyclic reactions

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [TS 87/15-1, TS 87/17-1]
  2. Interdisciplinary Center for Molecular Materials (ICMM)
  3. Erlangen Catalysis Resource Center (ECRC)
  4. Friedrich-Ebert-Stiftung

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Over the last several years there has been a huge increase in the development and applications of new efficient organocatalysts for enantioselective pericyclic reactions, which represent one of the most powerful types of organic transformations. Among these processes are cycloaddition reactions (e.g., [3+2]; formal [3+3]; [4+2]; vinylogous [4+2] and 1,3-dipolar cycloadditions), which belong to the most utilized reactions in organic synthesis of complex nitrogen- and oxygen-containing heterocyclic molecules. This review presents the breakthrough realized in this field using chiral BINOL-derived phosphoric acids and N-triflyl phosphoramide organocatalysts.

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