A Sequential Pummerer−Diels−Alder Route for the Generation and Trapping of Furo[3,4-c]pyridines: Synthesis of Heterocyclic Analogues of 1-Arylnaphthalene Lignans-Reference-Cited by-同舟云学术

A Sequential Pummerer−Diels−Alder Route for the Generation and Trapping of Furo[3,4-c]pyridines: Synthesis of Heterocyclic Analogues of 1-Arylnaphthalene Lignans

Published:2003-08-14 Issue:18 Volume:68 Page:6919-6927
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sarkar Tarun K.¹,Panda Niranjan¹,Basak Sankar¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kharagpur-721302, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0344081

Reference24 articles.

1. Recent Advances in the Chemistry of Benzo[c]furans and Related Compounds

2. The domino cycloaddition/N-acyliminium ion cyclization cascade

3. Methyl 4,6-dichloro-3-diethylaminofuro[3,4-c]pyridine-1-car☐ylate: Synthesis of the first stable azaisobenzofuran by a Hamaguchi-Ibata reaction

4. Synthesis and Reactions of a Stable o-Quinoid 10-π-Electron System, Furo[3,4-c]pyridine

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