The assembly of beta-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, H
The assembly of beta-methylene-TAD, a metabolically stable analogue of the antitumor agent TAD, by the stepwise esterification of monodeprotected methylenebis-(phosphonate) benzyl esters under Mitsunobu conditions. [electronic resource] - Bioorganic & medicinal chemistry letters Nov 1999 - 3069-74 p. digital
Publication Type: Journal Article
0960-894X
10.1016/s0960-894x(99)00544-2 doi
Adenosine Diphosphate--analogs & derivatives
Antineoplastic Agents--chemical synthesis
Esterification
Magnetic Resonance Spectroscopy
Molecular Structure
Organophosphonates--chemistry
Phosphoric Diester Hydrolases--chemistry
Thiazoles--chemical synthesis
The assembly of beta-methylene-TAD, a metabolically stable analogue of the antitumor agent TAD, by the stepwise esterification of monodeprotected methylenebis-(phosphonate) benzyl esters under Mitsunobu conditions. [electronic resource] - Bioorganic & medicinal chemistry letters Nov 1999 - 3069-74 p. digital
Publication Type: Journal Article
0960-894X
10.1016/s0960-894x(99)00544-2 doi
Adenosine Diphosphate--analogs & derivatives
Antineoplastic Agents--chemical synthesis
Esterification
Magnetic Resonance Spectroscopy
Molecular Structure
Organophosphonates--chemistry
Phosphoric Diester Hydrolases--chemistry
Thiazoles--chemical synthesis