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Volumn 40, Issue 33, 1999, Pages 5961-5965

Solid-state NMR and X-ray diffractional analysis of conformational effects in σ-symmetric bicyclo[2.2.1]hept-2-ene diester and monoesters

Author keywords

Bicyclic aliphatic compounds; Conformation; NMR; X ray crystal structures

Indexed keywords

NORBORNENE DERIVATIVE;

EID: 0033551748     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01151-X     Document Type: Article
Times cited : (6)

References (23)
  • 20
    • 0009591848 scopus 로고    scopus 로고
    • note
    • -3. The final refinement converged to R=0.066, wR=0.223 for 1265 [Fo>4σ(Fo)] reflections.
  • 21
    • 0009606475 scopus 로고    scopus 로고
    • note
    • 3OD. These decreased chemical shift differences suggest that the intramolecular H-bonding in 6 was disrupted in these protic solvents, in which the carboxyl and carbomethoxy groups have free rotation, and indicate the extent of the intramolecular H-bonding. We are grateful for the reviewer's suggestion of conducting this experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.