73410-59-0Relevant articles and documents
A CONVENIENT SYNTHESIS OF 6-, 7-, AND 8-MEMBERED CYCLIC PHOSPHODIESTERS
Ramirez, Fausto,Tsuboi, Hikotada,Okazaki, Hiroshi,Marecek, James F.
, p. 5375 - 5376 (1982)
1,3-, 1,4-, and 1,5-Alkanediols are converted into the corresponding 6-, 7-, and 8-membered cyclic phosphodiesters in a two-step procedure utilizing N-(1,2-dimethylethenylenedioxyphosphoryl)imidazole (2) as the sole phosphorylating reagent.
Influence of Phosphorus Derivatization on the Conformational Behavior of Model Compounds for 3',5'-xylo-cAMP Studied by 1H NMR Spectroscopy
Hermans, Rob J.M.,Buck, Henk M.
, p. 2077 - 2084 (2007/10/02)
A number of epimeric pairs of 3-X-3-Y-cis-2,4-dioxa-3-phosphabicyclononanes (2, X = OCH3, Y = O; 3, X = OCH3, Y = S; 4, X = OPh, Y = O; 5, X = OPh, Y = S; 6, X = Cl, Y = O; 7, X = Cl, Y = S; 8, X = N(CH3)2, Y = O; 9, X = N(CH3)2, Y = S; 10, X = Ss
Thermochemical Identification of the Structural Factors Responsible for the Thermodynamic Instability of 3',5'-Cyclic Nucleotides
Gerlt, John A.,Gutterson, Neal I.,Datta, Pradip,Belleau, Bernard,Penney, Christopher L.
, p. 1655 - 1660 (2007/10/02)
The enthalpies of hydrolysis of several cyclic phosphate diesters which can be considered to be structural analogues of the trans-fused trimethylene phosphate-ribofuranoside ring system of adenosine 3',5'-cyclic phosphate have been determined by microcalo
