90405-80-4Relevant academic research and scientific papers
Radical cyclisation onto C-3 of 1,6-anhydro-β-D-mannopyranose derivatives. Application to the formation of the C8a centre of (-)-tetrodotoxin
Noya, Beatriz,Alonso, Ricardo
, p. 2745 - 2748 (1997)
Starting from 1,6-anhydro-β-D-mannopyranose, compounds 7a-d, which have a ketoxime ether at C3 and a carbon radical precursor tethered to the hydroxyl group at position 2, were efficiently prepared. While alkyl π-radicals derived from 7a and 7b failed to cyclize, the vinyl σ-radicals derived from 7c and 7d underwent the desired 1,5-exo cyclization, affording advanced precursors of (-)-tetrodotoxin, This type of transformation should be useful for the formation of sterically crowded nitrogen-bearing carbon centers in carbohydrate-derived substrates.
5-exo Radical Cyclization onto 3-Alkoxyketimino-1,6-anhydromannopyranoses. Efficient Preparation of Synthetic Intermediates for (-)-Tetrodotoxin
Noya,Paredes,Ozores,Alonso
, p. 5960 - 5968 (2007/10/03)
Ketoxime ethers at C3 of 1,6-anhydro-β-D-mannopyranose derivatives were found to be useful 5-exo radical traps of alkyl and vinyl radicals generated at a chain tethered to the C2 hydroxyl group, allowing advanced synthetic intermediates for (-)-tetrodotoxin to be prepared from D-mannose in good overall yield.
