Isosteric Phosphonate Analogues of ET‐16‐OMe. Synthesis and Biological Evaluation of the Enantiomers of 2′‐(Trimethylammonio)ethyl 4‐( Hexadecyloxy)‐3‐methoxybutanephosphonate and 2′‐(Trimethylammonio) ethyl 4‐(Hexadecylthio)‐3‐methoxybutanephosphonate.
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R. Bittman | H. Salari | H. Byun | B. Mercier
[1] R. Bittman,et al. Isosteric phosphonate analogs of ET-16-OMe. Synthesis and biological evaluation of the enantiomers of 2'-(trimethylammonio)ethyl 4-(hexadecyloxy)-3-methoxybutanephosphonate and 2'-(trimethylammonio)ethyl 4-(hexadecylthio)-3-methoxybutanephosphonate. , 1994, Journal of medicinal chemistry.