80817-46-5Relevant academic research and scientific papers
Preparation of a disulfide-linked precipitative soluble support for solution-phase synthesis of trimeric oligodeoxyribonucleotide 3-(2-chlorophenylphosphate) building blocks
Jabgunde, Amit M.,Molina, Alejandro Gimenez,Virta, Pasi,L?nnberg, Harri,Flitsch
, p. 1553 - 1560 (2016/04/10)
The preparation of a disulfide-tethered precipitative soluble support and its use for solution-phase synthesis of tnmenc oligodeoxy-ribonucleotide 3′-(2-chlorophenylphosphate) building blocks is described. To obtain the building blocks, N-acyl protected 2
Synthesis of short oligodeoxyribonucleotides by phosphotriester chemistry on a precipitative tetrapodal support
Kungurtsev, Vyacheslav,Virta, Pasi,Loennberg, Harri
, p. 7886 - 7890 (2014/01/06)
Short oligodeoxyribonucleotides have been assembled from appropriately protected nucleoside 3′-(benzotriazol-1-yl 2-chlorophenyl phosphate) derivatives on hundred-milligram scales on a soluble tetrakis-O-(4- azidomethylphenyl)pentaerythritol support beari
New approach for the synthesis of c-di-GMP and its analogues
Amiot, Nicolas,Heintz, Karine,Giese, Bernd
, p. 4230 - 4236 (2008/09/17)
The synthesis of cyclic bis(3′-5′)diguanylic acid (c-di-GMP) by using a new flexible approach is reported. The flexibility of the method is exemplified by the synthesis of base-modified analogues that will find applications in the elucidation of c-di-GMP
REACTION BETWEEN NUCLEOSIDE BASE AND THE PHOSPHORYLATING AGENT DERIVED FROM 1-HYDROXYBENZOTRIAZOLE AND 2-CHLOROPHENYL PHOSPHORODICHLORIDATE
Reese, Colin B.,Richards, Keith H.
, p. 2245 - 2248 (2007/10/02)
In the presence of 1-methylimidazole, 2-N-acyl guanine (as in 4a), thymine (as in 5a), and uracil (as in 5b) residues react readily with the phosphorylating agent derived from 2-chlorophenyl phosphorodichloridate (1a) and 1-hydroxybenzotriazole.
A convenient method for the preparation of terminal methyl phosphates of nucleic acids
Wreesmann, C. T. J.,Hoogen, Y. Th. van den,Ledeboer, A. H.,Marel, G. A. van der,Boom, J. H. van
, p. 138 - 144 (2007/10/02)
The reagent 2-chlorophenyl bis(1-benzotriazolyl) phosphate has been used for the preparation of 5'-O-(methyl phosphate) esters of the dimers TpT, UpU, Upm62A and m62ApU, as well as 3',5'-bis-O-(methyl phosphate)esters of uridine (U)
SYNTHESIS OF A LIPOTEICHOIC ACID-CARRIER FRAGMENT OF Staphylococcus aureus
Oltvoort, Jan J.,Kloosterman, Marcel,Boeckel, Constant A. A. van,Boom, Jacques H. van
, p. 147 - 164 (2007/10/02)
A lipoteichoic acid-carrier fragment containing three glycerol units and one glycolipid unit was synthesized by use of the bifunctional phosphorylating reagents bis(1-benzotriazolyl) 2,2,2-tribromoethyl and 2-chlorophenyl phosphates.Protection of the sn-g
Improved Synthesis of Oligodeoxyribonucleotides by Solid-Phase Phosphotriester Method Utilizing O6--2'-deoxyguanosine Derivatives
Chollet, Andre,Ayala, Edgar,Kawashima, Eric H.
, p. 1356 - 1364 (2007/10/02)
The synthesis of oligodeoxyribonucleotides on a cross-linked polystyrene solid support utilizing stable mono- and dinucleotide phosphotriester building blocks is presented.The use of O6--2'deoxyguanosine derivatives yields cleaner DNA fragments by supressing side reactions.Modifications improving the phosphotriester methodology are presented.The purification methods and analysis of synthetic oligodeoxyribonucleotides are described.
Synthesis of a teichoic acid fragment of Bacillus subtilis using a modified phosphotriester approach
Boeckel, C. A. A. van,Visser, G. M.,Hermans, J. P. G.,Boom, J. H. van
, p. 526 - 537 (2007/10/02)
The synthesis of a teichoic acid fragment (i.e. compound 8e), containing three 3-O-(β-glucopyranosyl)-sn-glycerol residues connected via two phosphodiester linkages, is described.The assemblage of the teichoic acid fragment was effected using a modified p
A NEW APPROACH TO THE SYNTHESIS OF PHOSPHOTRIESTER INTERMEDIATES OF NUCLEOSIDES AND NUCLEIC ACIDS
Marel, G. van der,Boeckel, C.A.A. van,Wille, G.,Boom, J.H. van
, p. 3887 - 3890 (2007/10/02)
Aryl phosphorodichloridates can be converted by means of 1-hydroxybenzotriazole into an effective phosphorylating agent, which can be applied to the synthesis of phosphotriester intermediates of nucleic acids.
