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Volumn 52, Issue 26, 2011, Pages 3324-3328

A nontransmetalation reaction pathway for anionic four-electron donor-based palladacycle-catalyzed addition reactions of arylborons with aldehydes

Author keywords

Addition; Aldehydes; Arylboroxines; Transmetalation; Type I palladacycle

Indexed keywords

ALDEHYDE DERIVATIVE; BORON DERIVATIVE; ORGANOMETALLIC COMPOUND; TYPE I PALLADACYCLE; UNCLASSIFIED DRUG;

EID: 79957620156     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.04.074     Document Type: Article
Times cited : (12)

References (53)
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    • 68949151956 scopus 로고    scopus 로고
    • For recent reviews: N. Miyaura Synlett 2009 2039 2050
    • (2009) Synlett , pp. 2039-2050
    • Miyaura, N.1
  • 11
  • 37
    • 79957600168 scopus 로고    scopus 로고
    • Most Type I palladacycles are known to exist as bridged dimers and to dissociate into monomeric forms during reactions. Type I palladacycles in this Letter were drawn in monomeric forms
    • Most Type I palladacycles are known to exist as bridged dimers and to dissociate into monomeric forms during reactions. Type I palladacycles in this Letter were drawn in monomeric forms.
  • 48
    • 73249143142 scopus 로고    scopus 로고
    • For Ni(0)-catalyzed addition reactions of arylboroxines with aldehydes: C.-H. Xing, and Q.-S. Hu Tetrahedron Lett. 51 2010 924 927
    • (2010) Tetrahedron Lett. , vol.51 , pp. 924-927
    • Xing, C.-H.1    Hu, Q.-S.2
  • 49
    • 70350140363 scopus 로고    scopus 로고
    • For examples of the use of arylboronate esters as the nucleophile source for transition metal-catalyzed addition reactions in the absence of water: J. Bouffard, and K. Itami Org. Lett. 11 2009 4410 4413
    • (2009) Org. Lett. , vol.11 , pp. 4410-4413
    • Bouffard, J.1    Itami, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.