Synthesis of a maradolipid without using protecting groups
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- 作者：René ; Csuk ; rene.csuk@chemie.uni-halle.de ; Andrea Schultheiß ; Sven Sommerwerk ; Ralph Kluge
- 关键词：Maradolipid ; Chemoenzymatic trans-esterification ; Trehalose
- 刊名：Tetrahedron Letters
- 出版年：2013
- 出版时间：1 May, 2013
- 年：2013
- 卷：54
- 期：18
- 页码：2274-2276
- 全文大小：182 K
文摘
A convenient route has been developed to synthesize 6-O-mono- and 6,6¡ä-di-O-acyl symmetrical and unsymmetrical (un)-symmetrically trehalose derivatives from trehalose using a combination of enzymic and nonenzymic reactions. Thus, a typical maradolipid was accessed in two-steps.