Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1351028 | Tetrahedron: Asymmetry | 2005 | 5 Pages |
Abstract
An improved large-scale synthesis of 1,2:4,5-dianhydro-3-benzylarabitol and 1,2:4,5-dianhydroarabitol from arabitol is described.
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(2S,4S)-1,5-Di-O-(2,4,6-triisopropyl-benzenesulfonyl)-arabitolC35H56O9S2Ee = 100%[α]D24=-1.4 (c 2.2, CHCl3)Source of chirality: starting materialAbsolute configuration: (2S,4S)
(2S,4S)-1,2:4,5-Dianhydro-3-(benzyl)-arabitolC12H14O3Ee = 100%[α]D24=-27.8 (c 1.6, CHCl3)Source of chirality: starting materialAbsolute configuration: (2S,4S)
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Leo M.H. Leung, Vicky Gibson, Bruno Linclau,