Highly Exo-Selective Epoxidation and Hydroxylation of Triquinacene and Its Derivatives: All-exo-Hexahydroxytriquinane

Journal of Organic Chemistry

Volumn 63, Issue 8, 1998, Pages 2544-2547

  Haag, Rainer ^a   Zuber, Richard ^a   Donon, Sylvie ^b   Lee, Chi Hung ^a   Noltemeyer, Matthias ^a   Johnsen, Keyji ^a   De Meijere, Armin ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b SORBONNE UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000321878     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971796w     Document Type: Article

References (21)

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8. The definite proof that triquinacene is not a neutral homoaromatic system has recently been brought about by heat of combustion measurements: (a) Haag, R.; Kozhushkov, S. I.; de Meijere, A.; Beckhaus, H.-D.; Verewkin, S. P.; Rüchardt, C., in preparation; see also: (b) Storer, J. W.; Houk, K. N. J. Am. Chem. Soc. 1992, 114, 1165-1168.
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14. f = 0.45) were isolated.
15. The authors have deposited atomic coordinates for 4b and 9a with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Centre, 12 Union Road, CB2 1EZ, UK. (a) Sheldrick, G. M. Acta Crytallogr., Sect. A 1990, 46, 467. (b) Sheldrick, G. M, SHELXL-93, program for crystal structure refinement. University of Göttingen, 1993.
16. The authors have deposited atomic coordinates for 4b and 9a with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Centre, 12 Union Road, CB2 1EZ, UK. (a) Sheldrick, G. M. Acta Crytallogr., Sect. A 1990, 46, 467. (b) Sheldrick, G. M, SHELXL-93, program for crystal structure refinement. University of Göttingen, 1993.
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21. VanRheenen, V.; Kelly, R. C.; Cha, D. Y. Tetrahedron Lett. 1976, 1973-1976.