253682-74-5Relevant articles and documents
The assembly of β-methylene-TAD, a metabolically stable analogue of the antitumor agent TAD, by the stepwise esterification of monodeprotected methylenebis-(phosphonate) benzyl esters under Mitsunobu conditions
Ikeda, Hisafumi,Abushanab, Elie,Marquez, Victor E.
, p. 3069 - 3074 (2007/10/03)
Synthesis of the metabolically stable analogue of thiazole-4-carboxamide adenine dinucleotide (β-methylene-TAD) was achieved via the sequential monodeprotection of tetrabenzyl methylenebis(phosphonate) after two rounds of Mitsunobu esterifications with th