Structure, conformation, and stereodynamics of N-nitroso-2,4-diaryl-3-azabicyclo[3.3.1]nonanes and N-nitroso-2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ones

Journal of Organic Chemistry

Volumn 61, Issue 11, 1996, Pages 3766-3772

  Połoński, Tadeusz ^a   Pham, Marzena ^a   Milewska, Maria J ^a   Gdaniec, Maria ^b  

^a GDANSK UNIVERSITY OF TECHNOLOGY   (Poland)

^b ADAM MICKIEWICZ UNIVERSITY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 1542440286     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9600159     Document Type: Article

References (49)

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37. 1H NMR spectra. The weaker deshielding of the axial H-7 (at 2.22 and 2.08 ppm in 11a and 11b, respectively) than in the corresponding 2,4-diaryl derivatives is probably due to a flattening of the piperidine ring.
38. (a) The authors have deposited experimental details concerning the crystal structure determinations of 3b and 8b, atomic coordinates, anisotropic atomic displacement parameters of non-H atoms, and lists of bond lengths and angles with Cambridge Crystallographic Data Centre. The data can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, U.K.
39. 11b
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