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Volumn 29, Issue 22, 2010, Pages 5904-5911

Erratum: Oxidative addition of Sn-C bonds on palladium(0): Identification of palladium-stannyl species and a facile synthetic route to diphosphinostannylene-palladium complexes (Organometallics (2010) 29:22 5904-5911. DOI: 10.1021/om1007067);Oxidative addition of Sn-C bonds on palladium(0): Identification of palladium-stannyl species and a facile synthetic route to diphosphinostannylene- palladium complexes

Author keywords

[No Author keywords available]

Indexed keywords

CHLORINE COMPOUNDS; CRYSTAL ATOMIC STRUCTURE; ISOMERIZATION; ORGANOMETALLICS; PALLADIUM COMPOUNDS; SINGLE CRYSTALS; TIN COMPOUNDS; X RAY CRYSTALLOGRAPHY;

EID: 78649278858     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om500005y     Document Type: Erratum
Times cited : (20)

References (38)
  • 2
    • 0033441728 scopus 로고    scopus 로고
    • references therein.
    • Al-Allaf, T. A. K. Asian J. Chem. 1999, 11, 348, and references therein.
    • (1999) Asian J. Chem. , vol.11 , pp. 348
    • Al-Allaf, T.A.K.1
  • 4
    • 0030741227 scopus 로고    scopus 로고
    • Well-known examples are hydrostannylation and Stille-type cross-coupling. In the latter, the reaction of an activated alkynyltrialkyltin with a palladium(0)-iminophosphine precursor has been demonstrated to occur through oxidative addition of the Sn-alkynyl bond, which was claimed to be the first case of a Sn-C bond undergoing oxidative addition on palladium. Theoretical work has also been published on this system.
    • Well-known examples are hydrostannylation and Stille-type cross-coupling. In the latter, the reaction of an activated alkynyltrialkyltin with a palladium(0)-iminophosphine precursor has been demonstrated to occur through oxidative addition of the Sn-alkynyl bond, which was claimed to be the first case of a Sn-C bond undergoing oxidative addition on palladium. Theoretical work has also been published on this system. Shirakawa, E.; Yoshida, H.; Hiyama, T. Tetrahedron Lett. 1997, 38, 5177
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5177
    • Shirakawa, E.1    Yoshida, H.2    Hiyama, T.3
  • 9
    • 78649258975 scopus 로고    scopus 로고
    • These results were recently communicated at The 17th International Symposium on Homogeneous Catalysis (ISHC-17), July 2-9, Poznan, Poland.
    • These results were recently communicated at The 17th International Symposium on Homogeneous Catalysis (ISHC-17), July 2-9, 2010, Poznan, Poland.
    • (2010)
  • 11
    • 78649311436 scopus 로고    scopus 로고
    • note
    • 3 are most likely due to some protonolysis of the generated Pd-R bond (R = Me, H) by small quantities of HCl that are generated from hydrolysis of the starting alkyltin trichloride reagent by moisture.
  • 14
    • 0011416315 scopus 로고
    • Organotin trichlorides can easily act as chloride anion acceptors to form organotin tetrachloride anions.
    • Organotin trichlorides can easily act as chloride anion acceptors to form organotin tetrachloride anions. Dakternieks, D.; Zhu, H. Organometallics 1992, 11, 3820
    • (1992) Organometallics , vol.11 , pp. 3820
    • Dakternieks, D.1    Zhu, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.