Total synthesis of complex alkaloids by nucleophilic addition to amides

Takaaki Sato, Makoto Yoritate, Hayato Tajima, Noritaka Chida

Research output: Contribution to journalArticlepeer-review

89 Citations (Scopus)


Nucleophilic addition to amides has been recognized as a promising transformation for total synthesis of complex alkaloids. Amides can accept two different organometallic reagents through the nucleophilic addition, which enables it to serve as a stable surrogate of multi-substituted amines. However, the nucleophilic addition has been overlooked for a long time due to three main reasons: low electrophilicity of amide carbonyls, potential hydrolysis of the reaction intermediate and excess addition of an organometallic reagent. This mini review focuses on the recent progress of total synthesis of complex alkaloids based on the nucleophilic additions to N-alkoxyamides, tertiary amides and secondary amides.

Original languageEnglish
Pages (from-to)3864-3875
Number of pages12
JournalOrganic and Biomolecular Chemistry
Issue number21
Publication statusPublished - 2018
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry


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