Journal article

Palladium-catalyzed intramolecular O-arylation of enolates: application to benzo[b]furan synthesis.

Abstract:: [reaction: see text] A catalyst generated from Pd2(dba)3 and the ligand DPEphos effects intramolecular C-O bond formation between enolates and aryl halides in the conversion of 1-(2-haloaryl)ketones directly into the corresponding benzofurans. Both cyclic and acyclic ketones are efficient substrates. Thio ketones can also be employed allowing the preparation of the corresponding benzothiophenes.

Publication status:: Published

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APA Style

Willis, M., Taylor, D., & Gillmore, A. (2004). Palladium-catalyzed intramolecular O-arylation of enolates: application to benzo[b]furan synthesis. Organic Letters, 6(25), 4755–4757.

MLA Style

Willis, M, et al. “Palladium-Catalyzed Intramolecular O-Arylation of Enolates: Application to Benzo[b]Furan Synthesis.” Organic Letters, vol. 6, no. 25, 2004, pp. 4755–57.

Chicago Style

Willis, M, D Taylor, and A Gillmore. 2004. “Palladium-Catalyzed Intramolecular O-Arylation of Enolates: Application to Benzo[b]Furan Synthesis.” Organic Letters 6 (25): 4755–57.
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Publisher copy:: 10.1021/ol047993g

Authors

+ Willis, M More by this author

Role:: Author

+ Taylor, D More by this author

Role:: Author

+ Gillmore, A More by this author

Role:: Author

Journal:: Organic letters More from this journal
Volume:: 6
Issue:: 25
Pages:: 4755-4757
Publication date:: 2004-12-01
DOI:: 10.1021/ol047993g
EISSN:: 1523-7052
ISSN:: 1523-7060

Language:: English
Pubs id:: pubs:52462
UUID:: uuid:ee59917a-7b34-41af-9b69-5315befab3ad
Local pid:: pubs:52462
Source identifiers:: 52462
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_ee59917a7b3441af9b695315befab3ad

Terms of use

Copyright date:: 2004

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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