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

Publication type:	Article in scientific journal
Type of review:	Peer review (publication)
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
Authors:	Bolliger, Jeanne L. Frech, Christian M.
DOI:	10.1002/adsc.200900848
Published in:	Advanced Synthesis & Catalysis
Volume(Issue):	352
Issue:	6
Page(s):	1075
Pages to:	1080
Issue Date:	2010
Publisher / Ed. Institution:	Wiley
ISSN:	1615-4150 1615-4169
Language:	English
Subject (DDC):	540: Chemistry
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.
URI:	https://digitalcollection.zhaw.ch/handle/11475/10470
Fulltext version:	Published version
License (according to publishing contract):	Licence according to publishing contract
Departement:	Life Sciences and Facility Management
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.