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Volumn 19, Issue 8, 2013, Pages 2874-2888

Theory of the formation and decomposition of N-heterocyclic aminooxycarbenes through metal-assisted [2+3]-dipolar cycloaddition/retro- cycloaddition

Author keywords

cycloaddition; density functional calculations; isocyanides; N heterocyclic carbenes; reaction mechanisms

Indexed keywords

BACK DONATION; CARBENES; DIPOLAR CYCLOADDITIONS; HETEROCYCLES; HIGH ACTIVATION ENERGY; ISOCYANIDES; METAL CENTERS; N-HETEROCYCLIC; N-HETEROCYCLIC CARBENES; NITRONES; OXADIAZOLINES; PRINCIPAL FACTORS; REACTION MECHANISM;

EID: 84873627342     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201203098     Document Type: Article
Times cited : (46)

References (155)
  • 101
    • 46249102477 scopus 로고    scopus 로고
    • however, the mechanism and driving forces of the decomposition of oxadiazolines in accord with Scheme 1 are unknown to the best of our knowledge
    • G. Galvani, G. Calvet, N. Blanchard, C. Kouklovsky, Org. Biomol. Chem. 2008, 6, 1063; however, the mechanism and driving forces of the decomposition of oxadiazolines in accord with Scheme 1 are unknown to the best of our knowledge.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 1063
    • Galvani, G.1    Calvet, G.2    Blanchard, N.3    Kouklovsky, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.