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Volumn 29, Issue 3, 2010, Pages 624-629

Selective activation of benzylic carbon-hydrogen bonds of toluenes with rhodium(III) porphyrin methyl: Scope and mechanism

Author keywords

[No Author keywords available]

Indexed keywords

BENT TRANSITION STATE; BENZENE SOLVENT; BENZYLIC CARBON; BOND METATHESIS; HAMMETT PLOTS; HIGH YIELD; KINETIC ISOTOPE EFFECTS; LINEAR FREE ENERGY RELATIONSHIPS; NEGATIVE SLOPE; POSITIVE CHARGES; SELECTIVE ACTIVATION; SOLVENT FREE CONDITIONS; TRANSITION STATE;

EID: 76149094525     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9009119     Document Type: Article
Times cited : (19)

References (51)
  • 45
    • 76149086103 scopus 로고    scopus 로고
    • The 1,2-rearrangement rate of rhodium porphyrin alkyls with its rate-limiting β-hydride elimination step is enhanced by an electrondeficient porphyrin and is due to the resulting weaker Rh-C bond
    • The 1,2-rearrangement rate of rhodium porphyrin alkyls with its rate-limiting β-hydride elimination step is enhanced by an electrondeficient porphyrin and is due to the resulting weaker Rh-C bond.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.