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去氧红霉糖基urdamycin A的S-连接三糖缩醛糖的合成:发现硫氰酸烷基酯作为2-脱氧糖基锂立体选择性亚磺酰化的有效亲电试剂。

Synthesis of S-linked trisaccharide glycal of derhodinosylurdamycin A: Discovery of alkyl thiocyanate as an efficient electrophile for stereoselective sulfenylation of 2-deoxy glycosyl lithium.

作者信息

Acharya Padam P, Baryal Kedar N, Reno Cristin E, Zhu Jianglong

机构信息

Department of Chemistry and Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, OH 43606, United States.

Department of Chemistry and Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, OH 43606, United States.

出版信息

Carbohydr Res. 2017 Aug 7;448:103-109. doi: 10.1016/j.carres.2017.06.005. Epub 2017 Jun 15.

Abstract

Stereoselective synthesis of S-linked trisaccharide glycal of angucycline antitumor antibiotic derhodinosylurdamycin A is described. The synthesis has been accomplished employing our previously reported umpolung S-glycosylation strategy - stereoselective sulfenylation of 2-deoxy glycosyl lithium. It was found that sugar-derived thiocyanate was a better electrophile than corresponding asymmetric disulfide in this type of stereoselective sulfenylation.

摘要

描述了蒽环类抗肿瘤抗生素去氧红紫丝菌素A的S-连接三糖缩醛糖的立体选择性合成。该合成是采用我们先前报道的极性转换S-糖基化策略——2-脱氧糖基锂的立体选择性亚磺酰化来完成的。发现在这种立体选择性亚磺酰化中,糖衍生的硫氰酸盐比相应的不对称二硫化物是更好的亲电试剂。

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