Synthesis of 3-Substituted Quinolines via Transition-Metal-Catalyzed Reductive Cyclization of o-Nitro Baylis−Hillman Acetates-Reference-Cited by-同舟云学术

Synthesis of 3-Substituted Quinolines via Transition-Metal-Catalyzed Reductive Cyclization of o-Nitro Baylis−Hillman Acetates

Published:2003-07-09 Issue:16 Volume:68 Page:6427-6430
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

O'Dell David K.¹,Nicholas Kenneth M.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Oklahoma, 620 Parrington Oval, Norman, Oklahoma 73019 knicholas@ou.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034447c

Reference49 articles.

1. Balasubramanian, M.; Keay, J. G. InComprehensive HeterocyclicChemistry II; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Pergamon: Oxford, 1996; Vol. 5, Chapter 5.06, p 245.

2. Chemistry of Heterocyclic Compounds

3. Zn(II)-Mediated Alkynylation−Cyclization of o-Trifluoroacetyl Anilines: One-Pot Synthesis of 4-Trifluoromethyl-Substituted Quinoline Derivatives

4. Novel Synthesis of 2-Chloroquinolines from 2-Vinylanilines in Nitrile Solvent

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