Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne–carbonyl metathesis

Maloy Nayak; Ikyon Kim

doi:10.1039/c5ob01383f

journal article Jan 01, 2015

Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne–carbonyl metathesis

Maloy Nayak Ikyon Kim

Organic & Biomolecular Chemistry Vol. 13 No. 37 pp. 9697-9708 · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/c5ob01383f

Abstract

The strategic use of a sequential Sonogashira coupling/intramolecular alkyne–carbonyl metathesis process for the synthesis of a pyridine ring from 1-(2-haloaryl)-1H-pyrrole-2-carbaldehydes allowed ready access to diverse novel benzo-fused indolizines, pyrrolo[1,2-a]quinolines, in good to excellent yields.

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References

Details

Published: Jan 01, 2015
Vol/Issue: 13(37)
Pages: 9697-9708

Authors

M

Maloy Nayak

College of Pharmacy and Yonsei Institute of Pharmaceutical Sciences; Yonsei University; Incheon 406-840; Republic of Korea

I

Ikyon Kim

College of Pharmacy and Yonsei Institute of Pharmaceutical Sciences; Yonsei University; Incheon 406-840; Republic of Korea

Cite This Article

Maloy Nayak, Ikyon Kim (2015). Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne–carbonyl metathesis. Organic & Biomolecular Chemistry, 13(37), 9697-9708. https://doi.org/10.1039/c5ob01383f

Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne–carbonyl metathesis

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