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A facile synthetic approach to access of 3H-pyrrolo[2,3-c]quinoline derivatives has been achieved by a sequential I2-promoted cyclization/Staudinger/aza-Wittig/dehydroaromatization reaction. The targeted products were received in moderate to good yields (62–81%). The… Click to show full abstract
A facile synthetic approach to access of 3H-pyrrolo[2,3-c]quinoline derivatives has been achieved by a sequential I2-promoted cyclization/Staudinger/aza-Wittig/dehydroaromatization reaction. The targeted products were received in moderate to good yields (62–81%). The broad substrate scope and easy availability of the starting materials make this method a valuable tool for generating 3H-pyrrolo[2,3-c]quinoline products.
Keywords:
pyrrolo quinoline;
sequential promoted;
staudinger aza;
cyclization staudinger;
quinoline;
promoted cyclization
Journal Title: Synlett
Year Published: 2019
Link to full text (if available)
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Journal Title: Synlett
Year Published: 2019
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!