4.7 Article

BF3-promoted reactions of α-amino acetals with alkynes to 2,5-disubstituted pyrroles

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 12, Pages 3317-3321

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo00405d

Keywords

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Funding

  1. Nanjing Tech University
  2. Fundamental Research Funds for the Central Universities [D5000210701]
  3. Ministry of Education of Singapore [M4012045.110, RG12/18-S]

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An efficient BF3-promoted cyclization reaction has been developed for the synthesis of substituted pyrroles using easily accessible alpha-amino acetals as starting materials. This metal-free process can be carried out under mild conditions.
An efficient BF3-promoted cyclization of alpha-amino acetals with alkynes for the assembly of substituted pyrroles has been developed. This cascade process uses easily accessible alpha-amino acetals as raw materials and can be achieved under mild conditions through a simple metal-free operation.

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