Canas-Rodriguez A, Ruiz-Poveda S G
Carbohydr Res. 1977 Oct;58(2):379-85. doi: 10.1016/s0008-6215(00)84364-5.
3',4',5,6-Tetradoxyneamine (7) was synthesized from neamine by the reaction sequence N-acetylation, O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hyrolysis, Alternatively, 7 was obtained by treatment of tetra-(N-methoxycarbonyl)neamine with sulphuryl chloride, followed by hydrogenation in the presence of palladium-on-charcoal and triethylamine, and removal of the N-protecting groups. 5,6-Dideoxyneamine (11) was synthesized from known 5,6-O-cyclohexylidene-tetra-(N-methoxycarbonyl)neamine by the reaction sequence 3',4'-O-acetylation, removal of the 5,6-O-cyclohexylidene group, 5,6-di-O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hydrolysis. An alternative route involved treatment of 3',4'-di-O-acetyl-tetra-(N-methoxycarbonyl)-neamine (8) with sulphuryl chloride, hydrogenation of the product, and removal of the protecting groups to give 11.
3',4',5,6 - 四脱氧新霉素胺(7)由新霉素通过N - 乙酰化、O - 甲磺酰化、用碘化钠 - 锌粉处理、氢化和碱水解的反应序列合成。另外,7也可通过用硫酰氯处理四 -(N - 甲氧羰基)新霉素,然后在钯 - 炭和三乙胺存在下氢化,并除去N - 保护基团而得到。5,6 - 二脱氧新霉素胺(11)由已知的5,6 - O - 环己叉基 - 四 -(N - 甲氧羰基)新霉素通过3',4'-O - 乙酰化、除去5,6 - O - 环己叉基、5,6 - 二 - O - 甲磺酰化、用碘化钠 - 锌粉处理、氢化和碱水解的反应序列合成。另一条路线涉及用硫酰氯处理3',4'-二 - O - 乙酰基 - 四 -(N - 甲氧羰基) - 新霉素(8),将产物氢化,并除去保护基团以得到11。