Stereoselective cyclisation of the 2-allyloxytetrahydropyran-3-yl radical and related species: The influence of anomeric effects
ALJ Beckwith, DM Page
Index: Beckwith, Athelstan L. J.; Page, Dennis M. Tetrahedron, 1999 , vol. 55, # 11 p. 3245 - 3254
Full Text: HTML
Citation Number: 11
Abstract
Ring closures of the 2-allyloxytetrahydropyran-3-yl radical 1b, its mono-oxa analog 1d and the all carbon system 1a give mainly the cis-fused syn-substituted bicyclononylcarbinyl radicals 2b, 2d and 2a, but the mono-oxa radical 1c gives mainly the cis-fused anti- substituted radical 3c. Molecular mechanics calculations show that the unexpected failure of the dioxa radical 1b to reflect the influence of the anomeric effect on the stereochemistry of ...
Related Articles:
[Van Rijn, Jimmy A.; Guijt, Marieke C.; De Vries, Dwight; Bouwman, Elisabeth; Drent, Eite Applied Organometallic Chemistry, 2011 , vol. 25, # 3 p. 212 - 219]
[Ferber, Peter H.; Gream, George E.; Stoneman, Terry I. Australian Journal of Chemistry, 1985 , vol. 38, # 5 p. 699 - 711]
[Ferber, Peter H.; Gream, George E.; Stoneman, Terry I. Australian Journal of Chemistry, 1985 , vol. 38, # 5 p. 699 - 711]
[Ferber, Peter H.; Gream, George E.; Stoneman, Terry I. Australian Journal of Chemistry, 1985 , vol. 38, # 5 p. 699 - 711]
[Cookson,R.C.; Wallis,S.R. Journal of the Chemical Society [Section] B: Physical Organic, 1966 , p. 1245 - 1256]