作者:Mohammed Benazza、Daniel Beaupère、Raoul Uzan、Gilles Demailly
DOI:10.1016/0008-6215(91)84087-u
日期:1991.9
Methanesulfonyl chloride in N,N-dimethylformamide transformed unprotected D-arabinitol into its 1,5-dichloro derivative in 50% yield. Other pentitols also reacted to give the corresponding 1,5-dichloropentitols, but with lower yields. The structures of the products were determined by n.m.r. spectroscopy.