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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.

Authors+Show Affiliations

Faculty of Engineering and Graduate School of Science and Technology, Niigata University, 8050, 2-Nocho, Ikarashi, Nishi-ku, Niigata 950-2181, Japan. hoshi@gs.niigata-u.ac.jpNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

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 -