Catalytic synthesis of enantiopure mixed diacylglycerols – synthesis of a major M. tuberculosis phospholipid and platelet activating factor
作者:Peter Fodran、Adriaan J. Minnaard
DOI:10.1039/c3ob41483c
日期:——
An efficient catalytic one-pot synthesis of TBDMS-protected diacylglycerols has been developed, starting from enantiopure glycidol. Subsequent migration-free deprotection leads to stereo- and regiochemically pure diacylglycerols. This novel strategy has been applied to the synthesis of a major Mycobacterium tuberculosis phospholipid, its desmethyl analogue, and platelet activating factor.
一种高效催化的一锅法合成TBDMS保护的二酰基甘油已被开发出来,从手性纯甘油酸环丙烷开始,随后无迁移的脱保护步骤产生立体化学和区域化学纯的二酰基甘油。这种新颖的策略已应用于合成主要的结核分枝杆菌磷脂、其脱甲基类似物和血小板活化因子。