摘要
在微波辐射下,葡萄糖烯(1)与硝酮2环加成反应的效率大大提到,在乙二醇二甲醚溶液中,200℃封管反应2min,环加成反应产物的收率可高达96%,而且反应的立体选择性无明显变化.利用环加成产物可进一步合成各种含官能团的碳糖苷衍生物,找到了一种合成碳糖苷衍生物中间体的简便有效方法.
With microwave irradiation, the efficiency of the 1,3-dipolar cycloaddition of exo-glucal (1) with nitrones 2 was remarkably improved, and the yield of the microwave assisted reaction in a seamless pressure vial at 200 ℃ for 2 min could be up to 96%, providing a practical and convenient method for preparing spiro-isoxazolidine glycosides which are very important intermediates for synthesizing various C-glycosides possessing functional groups.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2008年第10期1750-1755,共6页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(Nos.20472015
20672027)
河北省自然科学基金(Nos.B2005000106
B2008000588)
教育部科学技术研究重点(No.206013)资助项目.
关键词
微波促进
1
3-偶极环加成反应
外糖烯
硝酮
螺异嗯唑烷糖苷
microwave assisted
1,3-dipolar cycloaddition
exo-glycal
nitrone
spiro-isoxazolidine glyco- side