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.
Links
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 -