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Rhodium-catalyzed annulation of ynamides with bifunctional arylboron reagents.
Org Lett. 2010 Jun 04; 12(11):2554-7.OL

Abstract

Annulation of ynamides with arylboronic acids or esters containing an electrophilic functional group at the ortho-position proceeds under the action of rhodium catalysis to generate 2-amidoindenols or 2-amidoindenes, usually with good regioselectivity.

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Authors+Show Affiliations

Gourdet B
School of Chemistry, University of Edinburgh, The King's Buildings, West Mains Road, Edinburgh EH9 3JJ, UK.
Rudkin ME
No affiliation info available
Lam HW
No affiliation info available

MeSH

AlkynesBoronic AcidsCatalysisCyclizationEstersIndenesMolecular StructureRhodium

Pub Type(s)

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

Language

eng

PubMed ID

20446723

Citation

Gourdet, Benoit, et al. "Rhodium-catalyzed Annulation of Ynamides With Bifunctional Arylboron Reagents." Organic Letters, vol. 12, no. 11, 2010, pp. 2554-7.
Gourdet B, Rudkin ME, Lam HW. Rhodium-catalyzed annulation of ynamides with bifunctional arylboron reagents. Org Lett. 2010;12(11):2554-7.
Gourdet, B., Rudkin, M. E., & Lam, H. W. (2010). Rhodium-catalyzed annulation of ynamides with bifunctional arylboron reagents. Organic Letters, 12(11), 2554-7. https://doi.org/10.1021/ol100769p
Gourdet B, Rudkin ME, Lam HW. Rhodium-catalyzed Annulation of Ynamides With Bifunctional Arylboron Reagents. Org Lett. 2010 Jun 4;12(11):2554-7. PubMed PMID: 20446723.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Rhodium-catalyzed annulation of ynamides with bifunctional arylboron reagents. AU - Gourdet,Benoit, AU - Rudkin,Mairi E, AU - Lam,Hon Wai, PY - 2010/5/8/entrez PY - 2010/5/8/pubmed PY - 2010/8/18/medline SP - 2554 EP - 7 JF - Organic letters JO - Org Lett VL - 12 IS - 11 N2 - Annulation of ynamides with arylboronic acids or esters containing an electrophilic functional group at the ortho-position proceeds under the action of rhodium catalysis to generate 2-amidoindenols or 2-amidoindenes, usually with good regioselectivity. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/20446723/Rhodium_catalyzed_annulation_of_ynamides_with_bifunctional_arylboron_reagents_ L2 - https://doi.org/10.1021/ol100769p DB - PRIME DP - Unbound Medicine ER -