Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-<scp>d</scp>-hexopyranoses with diethylaminosulphur trifluoride
作者:Jindřich Karban、Ivana Císařová、Tomáš Strašák、Lucie Červenková Šťastná、Jan Sýkora
DOI:10.1039/c1ob06336g
日期:——
A complete series of eight 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses were subjected to fluorination with DAST. The 1,6:3,4-dianhydropyranoses yielded solely products of skeletal rearrangement resulting from migration of the tetrahydropyran oxygen (educts of D-altro and D-talo configuration) or of the 1,6-anhydro bridge oxygen (D-allo, D-galacto). The major products yielded by the 1,6:2,3-dianhydropyranoses
用DAST对8个1,6:2,3-和1,6:3,4-二脱水-β - D-己吡喃糖的完整系列进行氟化。1,6-:3,4-dianhydropyranoses产生从四氢吡喃氧迁移所得的(离析物的骨架重排的单独的产品d -雅卓和d - TALO配置)或1,6-脱水桥氧的(d -异体,D - galacto)。由1,6得到的主要产物:2,3- dianhydropyranoses来自亲核取代而产生的化合物,具有配置在C4任一保留(d -距骨,d -gulo)或倒置(D - manno),或来自C6迁移(D - allo)。1,6:2,3系列中的次要产物是由四氢吡喃氧(D - gulo)或环氧乙烷氧(D - manno)迁移或亲核取代并保留构型(D - manno)产生的。大多数重排产物的结构通过X射线晶体学证实。