Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines.Org Lett. 2011 Oct 07; 13(19):5314-7.OL
Abstract
A regio- and stereoselective rhodium-catalyzed synthesis of trisubstituted allylic alcohols is described. The utility of these synthons is demonstrated in a convenient synthesis of indenes and quinolines.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
21916430
Citation
Panteleev, Jane, et al. "Addition of Arylboronic Acids to Arylpropargyl Alcohols En Route to Indenes and Quinolines." Organic Letters, vol. 13, no. 19, 2011, pp. 5314-7.
Panteleev J, Huang RY, Lui EK, et al. Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines. Org Lett. 2011;13(19):5314-7.
Panteleev, J., Huang, R. Y., Lui, E. K., & Lautens, M. (2011). Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines. Organic Letters, 13(19), 5314-7. https://doi.org/10.1021/ol202176g
Panteleev J, et al. Addition of Arylboronic Acids to Arylpropargyl Alcohols En Route to Indenes and Quinolines. Org Lett. 2011 Oct 7;13(19):5314-7. PubMed PMID: 21916430.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines.
AU - Panteleev,Jane,
AU - Huang,Richard Y,
AU - Lui,Erica K J,
AU - Lautens,Mark,
Y1 - 2011/09/14/
PY - 2011/9/16/entrez
PY - 2011/9/16/pubmed
PY - 2012/1/18/medline
SP - 5314
EP - 7
JF - Organic letters
JO - Org Lett
VL - 13
IS - 19
N2 - A regio- and stereoselective rhodium-catalyzed synthesis of trisubstituted allylic alcohols is described. The utility of these synthons is demonstrated in a convenient synthesis of indenes and quinolines.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/21916430/Addition_of_arylboronic_acids_to_arylpropargyl_alcohols_en_route_to_indenes_and_quinolines_
L2 - https://doi.org/10.1021/ol202176g
DB - PRIME
DP - Unbound Medicine
ER -