Dipartimento di Scienze Farmaceutiche, Università di Pisa, Via Bonanno, 33 I-56126 Pisa, Italy.
Carbohydr Res. 2010 Feb 11;345(3):369-76. doi: 10.1016/j.carres.2009.11.027. Epub 2009 Nov 26.
Partially protected derivatives of L-ribo- and D-lyxo-aldohexos-5-ulose have been prepared starting from triacetonlactose dimethyl acetal derivatives. Key steps of the synthetic sequences are (a) the synthesis of 4'-deoxy-4'-eno- and 6'-deoxy-5'-eno lactose derivatives, and (b) the epoxidation-methanolysis of the above-mentioned enol ethers to give 1,5-bis-glycopyranosides, masked form of the target 1,5-dicarbonyl hexoses.
部分保护的 L-核糖和 D-来苏戊醛-5-酮的衍生物已从三乙酰基乳糖二甲缩醛衍生物开始制备。合成序列的关键步骤是:(a)合成 4'-去氧-4'-烯和 6'-去氧-5'-烯乳糖衍生物,和(b)上述烯醚的环氧化-甲醇解,得到 1,5-双糖苷,即目标 1,5-二羰基己糖的掩蔽形式。