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Volumn 4, Issue 11, 2011, Pages 1613-1621

Peculiarities of β-pinene autoxidation

Author keywords

autoxidation; kinetics; radical reactions; renewable resources; singlet oxygen

Indexed keywords

ANTIGEN-ANTIBODY REACTIONS; ATOMS; ENZYME KINETICS; KETONES; MOLECULAR OXYGEN; MONOTERPENES; THERMOOXIDATION;

EID: 81255177679     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.201100266     Document Type: Article
Times cited : (36)

References (53)
  • 2
    • 76349093792 scopus 로고    scopus 로고
    • Food and Agriculture Organisation of the United Nations, Rome
    • Pulp and Paper Capacities, Food and Agriculture Organisation of the United Nations, Rome, 2008.
    • (2008) Pulp and Paper Capacities
  • 20
    • 0033732231 scopus 로고    scopus 로고
    • The resulting radical is tertiary and benefits from hyperconjugation of the cyclobutyl group. For unactivated olefins, such as propene, opposite selectivities have been computationally postulated:, However, it would be difficult to verify experimentally that claim, since the formed intermediate quickly rearranges into epoxide
    • The resulting radical is tertiary and benefits from hyperconjugation of the cyclobutyl group. For unactivated olefins, such as propene, opposite selectivities have been computationally postulated:, C. C. Chen, J. W. Bozzelli, J. Phys. Chem. A 2000, 104, 4997. However, it would be difficult to verify experimentally that claim, since the formed intermediate quickly rearranges into epoxide.
    • (2000) J. Phys. Chem. A , vol.104 , pp. 4997
    • Chen, C.C.1    Bozzelli, J.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.