The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance

Bolliger, Jeanne L.; Frech, Christian M.

doi:10.1002/adsc.200900848

Full metadata record

DC Field	Value	Language
dc.contributor.author	Bolliger, Jeanne L.	-
dc.contributor.author	Frech, Christian M.	-
dc.date.accessioned	2018-09-12T12:49:20Z	-
dc.date.available	2018-09-12T12:49:20Z	-
dc.date.issued	2010	-
dc.identifier.issn	1615-4150	de_CH
dc.identifier.issn	1615-4169	de_CH
dc.identifier.uri	https://digitalcollection.zhaw.ch/handle/11475/10470	-
dc.description.abstract	The rapidly prepared 1,3‐diaminobenzene‐derived aminophosphine pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} is an effective Suzuki catalyst with excellent functional group tolerance. Side‐product formations, such as homocoupling, debromation or protodeboration have only rarely been detected and if so, were in all cases below the 5% level. The presented reaction protocol is universally applicable.	de_CH
dc.language.iso	en	de_CH
dc.publisher	Wiley	de_CH
dc.relation.ispartof	Advanced Synthesis & Catalysis	de_CH
dc.rights	Licence according to publishing contract	de_CH
dc.subject.ddc	540: Chemie	de_CH
dc.title	The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance	de_CH
dc.type	Beitrag in wissenschaftlicher Zeitschrift	de_CH
dcterms.type	Text	de_CH
zhaw.departement	Life Sciences und Facility Management	de_CH
dc.identifier.doi	10.1002/adsc.200900848	de_CH
zhaw.funding.eu	No	de_CH
zhaw.issue	6	de_CH
zhaw.originated.zhaw	No	de_CH
zhaw.pages.end	1080	de_CH
zhaw.pages.start	1075	de_CH
zhaw.publication.status	publishedVersion	de_CH
zhaw.volume	352	de_CH
zhaw.publication.review	Peer review (Publikation)	de_CH
Appears in collections:	Publikationen Life Sciences und Facility Management

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Bolliger, J. L., & Frech, Christian M. (2010). The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance. Advanced Synthesis & Catalysis, 352(6), 1075–1080. https://doi.org/10.1002/adsc.200900848

Bolliger, J.L. and Frech, Christian M. (2010) ‘The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance’, Advanced Synthesis & Catalysis, 352(6), pp. 1075–1080. Available at: https://doi.org/10.1002/adsc.200900848.

J. L. Bolliger and Christian M. Frech, “The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance,” Advanced Synthesis & Catalysis, vol. 352, no. 6, pp. 1075–1080, 2010, doi: 10.1002/adsc.200900848.

BOLLIGER, Jeanne L. und Christian M. FRECH, 2010. The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : a highly active Suzuki-Miyaura catalyst with excellent functional group tolerance. Advanced Synthesis & Catalysis. 2010. Bd. 352, Nr. 6, S. 1075–1080. DOI 10.1002/adsc.200900848

Bolliger, Jeanne L., and Christian M. Frech. 2010. “The 1,3-Diaminobenzene-Derived Aminophosphine Palladium Pincer Complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : A Highly Active Suzuki-Miyaura Catalyst with Excellent Functional Group Tolerance.” Advanced Synthesis & Catalysis 352 (6): 1075–80. https://doi.org/10.1002/adsc.200900848.

Bolliger, Jeanne L., and Christian M. Frech. “The 1,3-Diaminobenzene-Derived Aminophosphine Palladium Pincer Complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} : A Highly Active Suzuki-Miyaura Catalyst with Excellent Functional Group Tolerance.” Advanced Synthesis & Catalysis, vol. 352, no. 6, 2010, pp. 1075–80, https://doi.org/10.1002/adsc.200900848.