Issue 8, 2024

Silylacetate-promoted addition reaction of isocyanides to nitrones: effective synthesis of C(1)-carboxamide derivatives

Abstract

We report an efficient method for the synthesis of C(1)-carboxamide derivatives by adding isocyanides to 3,4-dihydroisoquinoline N-oxides and 3,4-dihydro-β-carboline 2-oxide in the presence of TMSOAc. 3,4-Dihydroisoquinoline-1-carboxylamide derivatives and 9-dihydro-3H-pyrido[3,4-b]indole-1-carboxamide derivatives were obtained in reasonable yields. The method could be used to synthesize alangiobussine, an alkaloid, in 61% yield.

Graphical abstract: Silylacetate-promoted addition reaction of isocyanides to nitrones: effective synthesis of C(1)-carboxamide derivatives

Supplementary files

Article information

Article type
Communication
Submitted
30 Oct 2023
Accepted
29 Jan 2024
First published
30 Jan 2024

Org. Biomol. Chem., 2024,22, 1619-1623

Silylacetate-promoted addition reaction of isocyanides to nitrones: effective synthesis of C(1)-carboxamide derivatives

T. Soeta, S. Yao, H. Sugiyama and Y. Ukaji, Org. Biomol. Chem., 2024, 22, 1619 DOI: 10.1039/D3OB01777J

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