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Volumn 21, Issue 5, 2010, Pages 909-914

Azabicyclo[3.3.1]nonanone: A case when weak interactions are preferred over strong hydrogen bonds

Author keywords

Azabicyclo 3.3.1 nonanone; Azatricyclo 7.3.1.02,7 trideca trienone; CH Pi interactions; Crystal engineering; Crystal structure and prediction; NH Pi interactions; Strong and weak intermolecular interactions

Indexed keywords


EID: 77956873181     PISSN: 10400400     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11224-010-9624-8     Document Type: Article
Times cited : (5)

References (17)
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    • S. E. Denmark and J. S. Siegel (Eds.), New Jersey: John Wiley
    • Nishio M, Umezava Y (2006) In: Denmark SE, Siegel JS (eds) Topics in stereochemistry, vol 25. John Wiley, New Jersey, pp 255-302.
    • (2006) Topics in Stereochemistry , vol.25 , pp. 255-302
    • Nishio, M.1    Umezava, Y.2
  • 11
    • 85050289539 scopus 로고
    • E. L. Eliel and N. Allinger (Eds.), New Jersey: John Wiley
    • Duax WL, Weeks CM, Rohrer DC (1976) In: Eliel EL, Allinger N (eds) Topics in stereochemistry, vol 9. John Wiley, New Jersey, pp 271-383.
    • (1976) Topics in Stereochemistry , vol.9 , pp. 271-383
    • Duax, W.L.1    Weeks, C.M.2    Rohrer, D.C.3
  • 12
    • 84990465786 scopus 로고    scopus 로고
    • Zefirov NS, Palyulin VA (1991). In: Eliel EL, Wilen SH (eds) Topics in stereochemistry, vol 20. John Wiley, New Jersey, pp. 171-230.
  • 15
    • 77956877873 scopus 로고    scopus 로고
    • Bruker (2004). APEXII (Version 1. 08), SAINT-Plus (Version 7. 23A) and SADABS (Version 2004/1). Bruker AXS Inc., Madison, Wisconsin, USA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.