Intramolecular Arylation Reactions of Alkenes: A Flexible Approach to Chromans and Tetrahydroquinoline Derivatives-Reference-Cited by-同舟云学术

Intramolecular Arylation Reactions of Alkenes: A Flexible Approach to Chromans and Tetrahydroquinoline Derivatives

Published:2004-02-27 Issue:11 Volume:126 Page:3416-3417
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Barluenga José¹,Trincado Mónica¹,Rubio Eduardo¹,González José M.¹

Affiliation:

1. Instituto Universitario de Química Organometálica “Enrique Moles”-Unidad Asociada al C.S.I.C., Universidad de Oviedo, Julián Claveria, 8, 33006 Oviedo, Spain

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0397299

Reference12 articles.

1. Representative examples: (a) Synthesis of six-membered rings: McKillop, A.; Boulton, A. J. InComprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon: Oxford, 1984; Vol. 2, p 72. (b) Synthesis of indoles: Sundberg, R. J.Indoles; Academic Press: London, 1996; p 27.

2. Heterocycle synthesis by palladium catalysed cyclisation-anion capture processes. A powerful new strategy

3. Regioselective Synthesis of Substituted Naphthalenes: A Novel de Novo Approach Based on a Metal-Free Protocol for Stepwise Cycloaddition of o-Alkynylbenzaldehyde Derivatives with Either Alkynes or Alkenes

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