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- W1987156692 abstract "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-acyl-sn-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." @default.
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- W1987156692 date "2006-07-01" @default.
- W1987156692 modified "2023-10-16" @default.
- W1987156692 title "Synthesis of short and long chain cardiolipins" @default.
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- W1987156692 doi "https://doi.org/10.1016/j.tet.2006.04.071" @default.
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