One Pot Synthesis\nof C3-Sulfurized Imidazolo [1,2‑<i>a</i>] Pyridines

A facile and efficient annulation strategy was developed\nfrom easily\naccessible <i>a</i>-bromoketones, aminopyridines and benzazol,\nwhich afforded a series of imidazole [1,2-<i>a</i>]­pyridine\nsulfides in moderate to good yields. The reaction involves the formation\nof C–N/C–S bond with the advantages of easy operation\nand wide substrates scope.

Publication Details

Journal
Figshare
Published
2024-10-04
DOI
https://doi.org/10.1021/acs.joc.4c01524.s001
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

One Pot Synthesis\nof C3-Sulfurized Imidazolo [1,2‑a] Pyridines

Figshare
Sulfur-Based Synthesis Techniques
article

One Pot Synthesis\nof C3-Sulfurized Imidazolo [1,2‑a] Pyridines

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Abstract

A facile and efficient annulation strategy was developed\nfrom easily\naccessible <i>a</i>-bromoketones, aminopyridines and benzazol,\nwhich afforded a series of imidazole [1,2-<i>a</i>]­pyridine\nsulfides in moderate to good yields. The reaction involves the formation\nof C–N/C–S bond with the advantages of easy operation\nand wide substrates scope.

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Openalex Percentile: Top 70%
Sulfur-Based Synthesis Techniques
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One Pot Synthesis\nof C3-Sulfurized Imidazolo [1,2‑<i>a</i>] Pyridines · Figshare (2024) | TGRS Research Map | TGRS