B. Mercier

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.

R. Bittman, H. Salari, H. Byun, 1994, Journal of medicinal chemistry.

2'-(Trimethylammonio)ethyl 4-(hexadecyloxy)-3(S)-methoxybutanephosphonate: a novel potent antineoplastic agent.

R. Bittman, H. Salari, H. Byun, 1993, Journal of medicinal chemistry.

Online SPE UPLC-MS/MS method for the simultaneous determination of 33 psychoactive drugs from swab-collected human oral fluid samples

J. Jouzeau, N. Gambier, V. Gibaja, 2022, Analytical and Bioanalytical Chemistry.

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.

R. Bittman, H. Salari, H. Byun, 1994 .

2′‐(Trimethylammonio)ethyl 4‐(Hexadecyloxy)‐3(S)‐ methoxybutanephosphonate (I): A Novel Potent Antineoplastic Agent.

R. Bittman, H. Salari, H. Byun, 1994 .