Rhodium-catalyzed isomerization of unactivated alkynes to 1,3-dienes.Chem Commun (Camb). 2006 Sep 14CC
Abstract
A rhodium/binap complex has been found to effectively catalyze the isomerization of unactivated internal alkynes to the corresponding 1,3-dienes in the presence of an azomethine imine as the reaction promoter.
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
17047793
Citation
Shintani, Ryo, et al. "Rhodium-catalyzed Isomerization of Unactivated Alkynes to 1,3-dienes." Chemical Communications (Cambridge, England), 2006, pp. 3646-7.
Shintani R, Duan WL, Park S, et al. Rhodium-catalyzed isomerization of unactivated alkynes to 1,3-dienes. Chem Commun (Camb). 2006.
Shintani, R., Duan, W. L., Park, S., & Hayashi, T. (2006). Rhodium-catalyzed isomerization of unactivated alkynes to 1,3-dienes. Chemical Communications (Cambridge, England), (34), 3646-7.
Shintani R, et al. Rhodium-catalyzed Isomerization of Unactivated Alkynes to 1,3-dienes. Chem Commun (Camb). 2006 Sep 14;(34)3646-7. PubMed PMID: 17047793.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Rhodium-catalyzed isomerization of unactivated alkynes to 1,3-dienes.
AU - Shintani,Ryo,
AU - Duan,Wei-Liang,
AU - Park,Soyoung,
AU - Hayashi,Tamio,
Y1 - 2006/08/02/
PY - 2006/10/19/pubmed
PY - 2007/5/22/medline
PY - 2006/10/19/entrez
SP - 3646
EP - 7
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
IS - 34
N2 - A rhodium/binap complex has been found to effectively catalyze the isomerization of unactivated internal alkynes to the corresponding 1,3-dienes in the presence of an azomethine imine as the reaction promoter.
SN - 1359-7345
UR - https://www.unboundmedicine.com/medline/citation/17047793/Rhodium_catalyzed_isomerization_of_unactivated_alkynes_to_13_dienes_
L2 - https://doi.org/10.1039/b605368h
DB - PRIME
DP - Unbound Medicine
ER -