Concise Synthesis of Glycerophospholipids

被引:23
|
作者
Mukhopadhyay, Tufan K. [1 ]
Trauner, Dirk [2 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
[2] Univ Penn, Coll Arts & Sci, Dept Chem, Philadelphia, PA 19104 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 88卷 / 15期
关键词
LYSOPHOSPHATIDYLSERINE ANALOGS; ASYMMETRIC CATALYSIS; EPOXIDES; AGONISTS;
D O I
10.1021/acs.joc.2c02096
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Glycerophospholipids are major components of cellular membranes and provide important signaling molecules. Besides shaping membrane properties, some bind to specific receptors to activate biological pathways. Untangling the roles of individual glycerophospholipids requires clearly defined molecular species, a challenge that can be best addressed through chemical synthesis. However, glycerophospholipid syntheses are often lengthy due to the contrasting polarities found within these lipids. We now report a general strategy to quickly access glycerophos-pholipids via opening of a phosphate triester epoxide with carboxylic acids catalyzed by Jacobsen's Co(salen) complex. We show that this method can be applied to a variety of commercially available fatty acids, photoswitchable fatty acids, and other carboxylic acids to provide the corresponding glycerophosphate derivatives.
引用
收藏
页码:11253 / 11257
页数:5
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