Skraup−Doebner−Von Miller Quinoline Synthesis Revisited: Reversal of the Regiochemistry for γ-Aryl-β,γ-unsaturated α-Ketoesters-Reference-Cited by-同舟云学术

Skraup−Doebner−Von Miller Quinoline Synthesis Revisited: Reversal of the Regiochemistry for γ-Aryl-β,γ-unsaturated α-Ketoesters

Published:2006-07-19 Issue:17 Volume:71 Page:6592-6595
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wu Yan-Chao¹,Liu Li¹,Li Hui-Jing¹,Wang Dong¹,Chen Yong-Jun¹

Affiliation:

1. Center for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China, and Graduate School of Chinese Academy of Sciences, Beijing 100049, China %yjchen@iccas.ac.cn

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo060290n

Reference25 articles.

1. Ueber eine dem Chinolin homologe Base

2. CXLVII.—The Doebner-Miller quinaldine synthesis

3. (d) Manske, R. H. F.; Kulka, M.Organic Reactions;Adams, R.Ed.; John Why & Sons: New York; 1953, Vol. 7, p 59.

4. (e) Weissberger, A.; Taylor, E. C. InTheChemistry of Heterocyclic Compounds- Quinolines;Gurnos, J., Ed.; Stonebridge Press: Bristol, 1977; p 93.

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