Abstract
A one-pot, three-component cascade reaction between unprotected sugars, primary amines, and 3-oxoacetonitriles gave N-substituted 2,3,5-functionalized pyrroles or N-substituted 2,3,4-functionalized pyrroles in excellent yields and selectivities. The selectivity of the reaction was achieved by simple control of the sequence of substrate addition. The reaction showed a wide substrate scope, and various types of sugars, primary amines, and oxoacetonitriles reacted smoothly. The work demonstrates a highly desired simple reaction for embedding nitrogen into sugars to produce valuable N-heterocyclic compounds that are amenable to further modifications to natural products and drug intermediates.
Original language | English |
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Pages (from-to) | 12115-12131 |
Number of pages | 17 |
Journal | Journal of Organic Chemistry |
Volume | 87 |
Issue number | 18 |
DOIs | |
Publication status | Published - Sept 16 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 American Chemical Society. All rights reserved.
ASJC Scopus Subject Areas
- Organic Chemistry