作者:Shoukath M. Ali、Moghis U. Ahmad、Peter Koslosky、Krishnudu Kasireddy、U. Murali Krishna、Imran Ahmad
DOI:10.1016/j.tet.2006.04.071
日期:2006.7
A phosphoramidite approach using 2-cyanoethyl N,N-diisopropylchlorophosphoramidite was utilized for the first time to synthesize short chain cardiolipins. The approach was extended to synthesize long chain and their ether analogue. Optically active 1,2-di-O-acylsn-glycerol or 1,2-di-O-myristyl-sn-glycerol was coupled with phosphoramidite reagent and 2-benzyloxy-1,3-propanediol in presence of 1H-tetrazole, followed by in situ oxidation, to give the corresponding protected cardiolipin analogues. The above intermediates were converted into cardiolipin analogues in two steps by deprotection of cyanoethyl and benzyl groups. (c) 2006 Elsevier Ltd. All rights reserved.