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KOtBu-catalyzed protocol for the post-ugi synthesis of spiro-γ-lactam-pyrrolo[2,3-b]quinoline derivatives in one-pot
This presentation describes an efficient and facile preparation of a series of new spiro-γ-lactam-pyrrolo[2,3-b]quinoline scaffolds. The Ugi adducts obtained via four-component condensation of 2-chloroquinoline-3-carbaldehydes, amines, trans-cinnamic acids and isocyanides underwent metal-free KOtBu-...
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Published in: | Tetrahedron 2023-06, Vol.140, p.133452, Article 133452 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This presentation describes an efficient and facile preparation of a series of new spiro-γ-lactam-pyrrolo[2,3-b]quinoline scaffolds. The Ugi adducts obtained via four-component condensation of 2-chloroquinoline-3-carbaldehydes, amines, trans-cinnamic acids and isocyanides underwent metal-free KOtBu-catalyzed bis-annulation processes to afford a diastereomeric mixture of the desired tetracyclic building blocks in moderate to good yields.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2023.133452 |