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Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes.
Angew Chem Int Ed Engl. 2013 Apr 22; 52(17):4607-12.AC

Abstract

2,3-Disubstituted benzo[b]furans are prepared in one step from commercially available phenols and readily accessible unactivated internal alkynes (see scheme). This Pd-catalyzed oxidative annulation has a broad substrate scope and allows access to a wide range of benzo[b]furans.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Kuram MR
School of Chemistry, University of Hyderabad, Hyderabad, India.
Bhanuchandra M
No affiliation info available
Sahoo AK
No affiliation info available

MeSH

AlkynesBenzofuransCatalysisMolecular StructureOxidation-ReductionPalladiumPhenols

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

23526675

Citation

Kuram, Malleswara Rao, et al. "Direct Access to Benzo[b]furans Through Palladium-catalyzed Oxidative Annulation of Phenols and Unactivated Internal Alkynes." Angewandte Chemie (International Ed. in English), vol. 52, no. 17, 2013, pp. 4607-12.
Kuram MR, Bhanuchandra M, Sahoo AK. Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes. Angew Chem Int Ed Engl. 2013;52(17):4607-12.
Kuram, M. R., Bhanuchandra, M., & Sahoo, A. K. (2013). Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes. Angewandte Chemie (International Ed. in English), 52(17), 4607-12. https://doi.org/10.1002/anie.201210217
Kuram MR, Bhanuchandra M, Sahoo AK. Direct Access to Benzo[b]furans Through Palladium-catalyzed Oxidative Annulation of Phenols and Unactivated Internal Alkynes. Angew Chem Int Ed Engl. 2013 Apr 22;52(17):4607-12. PubMed PMID: 23526675.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes. AU - Kuram,Malleswara Rao, AU - Bhanuchandra,M, AU - Sahoo,Akhila K, Y1 - 2013/03/25/ PY - 2012/12/21/received PY - 2013/01/31/revised PY - 2013/3/26/entrez PY - 2013/3/26/pubmed PY - 2014/4/15/medline SP - 4607 EP - 12 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 52 IS - 17 N2 - 2,3-Disubstituted benzo[b]furans are prepared in one step from commercially available phenols and readily accessible unactivated internal alkynes (see scheme). This Pd-catalyzed oxidative annulation has a broad substrate scope and allows access to a wide range of benzo[b]furans. SN - 1521-3773 UR - https://www.unboundmedicine.com/medline/citation/23526675/Direct_access_to_benzo[b]furans_through_palladium_catalyzed_oxidative_annulation_of_phenols_and_unactivated_internal_alkynes_ L2 - https://doi.org/10.1002/anie.201210217 DB - PRIME DP - Unbound Medicine ER -