A Phosphine-Mediated Synthesis of 1,4-Oxazepine- and 1,5-Oxazocine-Based Sugar Hybrids from Deoxysugar Azides

被引:2
作者
Kurhade, Suresh E. [1 ,3 ]
Salunkhe, Videsh T. [1 ]
Siddaiah, V. [3 ]
Bhuniya, Debnath [1 ]
Reddy, D. Srinivasa [1 ,2 ]
机构
[1] Advinus Therapeut Ltd, Discovery Chem, Pune 411057, Maharashtra, India
[2] CSIR, Natl Chem Lab, Pune 411008, Maharashtra, India
[3] Andhra Univ, Dept Organ Chem, Visakhapatnam 530003, Andhra Pradesh, India
来源
SYNTHESIS-STUTTGART | 2011年 / 21期
关键词
tandem reactions; heterocycles; carbohydrates; alkynes; oxazepines; oxazocines; azides; BETA-D-GLUCOSE; POLYCYCLIC HETEROCYCLES; CYCLOADDITION REACTION; ENKEPHALIN; DESIGN; BRAIN; DERIVATIVES; SCAFFOLDS; GLYCATION; DELIVERY;
D O I
10.1055/s-0030-1260218
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient and convenient method was developed for the synthesis of novel 1,4-oxazepine- and 1,5-oxazocine-based sugar hybrids from readily available deoxysugar azides by means of tributylphosphine-mediated tandem reactions. The resulting glycoconjugates might be useful in increasing the diversity of sugar backbones, and could find applications as potential glycomimetics and in drug discovery.
引用
收藏
页码:3523 / 3529
页数:7
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