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Volumn , Issue 1, 2000, Pages 135-141

Kinetic study of thermolysis of diarylhomonaphthoquinones. Endolexo substituent and solvent effects

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; COLUMN CHROMATOGRAPHY; CRYSTALLIZATION; ISOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PYROLYSIS; RATE CONSTANTS; SOLVENTS; STEREOCHEMISTRY;

EID: 0033993078     PISSN: 03009580     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (55)
  • 34
    • 0010787036 scopus 로고    scopus 로고
    • The calculations by the PM3 method were performed with the MOPAC program (ver. 6) using a Cache Work-System
    • The calculations by the PM3 method were performed with the MOPAC program (ver. 6) using a Cache Work-System.
  • 42
    • 0000534419 scopus 로고    scopus 로고
    • note
    • A, so-called quasi π) by linear combinations of three p-orbitals. Accordingly, the conjugation energy is a maximum when the neighboring p-orbital axis is arranged parallel to the plane of the cyclopropane ring (bisected conformation), while the magnitude of interaction is a minimum for the perpendicular arrangement.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.