Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides.Org Lett. 2008 May 15; 10(10):2063-6.OL
Abstract
High activity in the palladium-catalyzed Suzuki-Miyaura reactions of aryl chlorides with arylboronic acids was furnished using biphenylene-substituted di- tert-butylruthenocenylphosphine (R-Phos) as a supporting ligand. Substrate combinations even for the construction of highly hindered tetra- ortho-substituted biaryls can be achieved in good to excellent yields with low catalyst loadings in short reaction times.
Links
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
18422322
Citation
Hoshi, Takashi, et al. "Biphenylene-substituted Ruthenocenylphosphine for Suzuki-Miyaura Coupling of Aryl Chlorides." Organic Letters, vol. 10, no. 10, 2008, pp. 2063-6.
Hoshi T, Nakazawa T, Saitoh I, et al. Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides. Org Lett. 2008;10(10):2063-6.
Hoshi, T., Nakazawa, T., Saitoh, I., Mori, A., Suzuki, T., Sakai, J., & Hagiwara, H. (2008). Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides. Organic Letters, 10(10), 2063-6. https://doi.org/10.1021/ol800567q
Hoshi T, et al. Biphenylene-substituted Ruthenocenylphosphine for Suzuki-Miyaura Coupling of Aryl Chlorides. Org Lett. 2008 May 15;10(10):2063-6. PubMed PMID: 18422322.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides.
AU - Hoshi,Takashi,
AU - Nakazawa,Taichi,
AU - Saitoh,Ippei,
AU - Mori,Ayako,
AU - Suzuki,Toshio,
AU - Sakai,Jun-ichi,
AU - Hagiwara,Hisahiro,
Y1 - 2008/04/19/
PY - 2008/4/22/pubmed
PY - 2008/7/17/medline
PY - 2008/4/22/entrez
SP - 2063
EP - 6
JF - Organic letters
JO - Org Lett
VL - 10
IS - 10
N2 - High activity in the palladium-catalyzed Suzuki-Miyaura reactions of aryl chlorides with arylboronic acids was furnished using biphenylene-substituted di- tert-butylruthenocenylphosphine (R-Phos) as a supporting ligand. Substrate combinations even for the construction of highly hindered tetra- ortho-substituted biaryls can be achieved in good to excellent yields with low catalyst loadings in short reaction times.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/18422322/Biphenylene_substituted_ruthenocenylphosphine_for_Suzuki_Miyaura_coupling_of_aryl_chlorides_
DB - PRIME
DP - Unbound Medicine
ER -