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Volumn 27, Issue 1, 2004, Pages 33-50

Kinetics of protodestannylation of substituted vinylstannanes

Author keywords

Functionalised vinylstannanes; Kinetics; NMR; Nucleophilic assistance; Protodestannylation

Indexed keywords

ACETIC ACID; ACID; ALKYL GROUP; ALPHA CARBON; ANION; BETA CARBON; CARBON; CARBOXYLIC ACID; CHLOROACETIC ACID; PROTON; TIN; TIN DERIVATIVE; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 3242716208     PISSN: 07921241     EISSN: 21910219     Source Type: Journal    
DOI: 10.1515/MGMC.2004.27.1.33     Document Type: Article
Times cited : (1)

References (47)
  • 1
    • 3242736821 scopus 로고
    • Patai S. (Ed.), Chapter 2, Wiley, New York
    • For a review see: (a) M. H. Abraham, P. L. Grellier in: Patai S. (Ed.), The Chemistry of Metal-Carbon Bond, Chapter 2, Wiley, New York 1978; (b) A. G. Davies, Organotin Chemistry, VCH, Weinheim, 1997.
    • (1978) The Chemistry of Metal-Carbon Bond
    • Abraham, M.H.1    Grellier, P.L.2
  • 2
    • 0004063249 scopus 로고    scopus 로고
    • VCH, Weinheim
    • For a review see: (a) M. H. Abraham, P. L. Grellier in: Patai S. (Ed.), The Chemistry of Metal-Carbon Bond, Chapter 2, Wiley, New York 1978; (b) A. G. Davies, Organotin Chemistry, VCH, Weinheim, 1997.
    • (1997) Organotin Chemistry
    • Davies, A.G.1
  • 38
    • 3242665467 scopus 로고    scopus 로고
    • note
    • For ratios of rate constants higher then 10, method C (see Experimental) does not provide reproducible results because the integral intensities obtained for the slower reacting compound practically do not change during the experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.