• Something wrong with this record ?

Nucleoside-O-Methyl-(H)-Phosphinates: Novel Monomers for the Synthesis of Methylphosphonate Oligonucleotides Using H-Phosphonate Chemistry

O. Kostov, O. Páv, I. Rosenberg,

. 2017 ; 70 (-) : 4.76.1-4.76.22. [pub] 20170918

Language English Country United States

Document type Journal Article

This unit comprises the straightforward synthesis of protected 2'-deoxyribonucleoside-O-methyl-(H)-phosphinates in both 3'- and 5'-series. These compounds represent a new class of monomers compatible with the solid-phase synthesis of oligonucleotides using H-phosphonate chemistry and are suitable for the preparation of both 3'- and 5'-O-methylphosphonate oligonucleotides. The synthesis of 4-toluenesulfonyloxymethyl-(H)-phosphinic acid as a new reagent for the preparation of O-methyl-(H)-phosphinic acid derivatives is described. © 2017 by John Wiley & Sons, Inc.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18024638
003      
CZ-PrNML
005      
20180712092655.0
007      
ta
008      
180709s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1002/cpnc.35 $2 doi
035    __
$a (PubMed)28921496
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Kostov, Ondřej $u Department of Bioorganic and Medicinal Chemistry, Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
245    10
$a Nucleoside-O-Methyl-(H)-Phosphinates: Novel Monomers for the Synthesis of Methylphosphonate Oligonucleotides Using H-Phosphonate Chemistry / $c O. Kostov, O. Páv, I. Rosenberg,
520    9_
$a This unit comprises the straightforward synthesis of protected 2'-deoxyribonucleoside-O-methyl-(H)-phosphinates in both 3'- and 5'-series. These compounds represent a new class of monomers compatible with the solid-phase synthesis of oligonucleotides using H-phosphonate chemistry and are suitable for the preparation of both 3'- and 5'-O-methylphosphonate oligonucleotides. The synthesis of 4-toluenesulfonyloxymethyl-(H)-phosphinic acid as a new reagent for the preparation of O-methyl-(H)-phosphinic acid derivatives is described. © 2017 by John Wiley & Sons, Inc.
650    _2
$a oligonukleotidy $x chemická syntéza $7 D009841
650    _2
$a organofosfonáty $7 D063065
650    _2
$a organofosforové sloučeniny $x chemie $7 D009943
655    _2
$a časopisecké články $7 D016428
700    1_
$a Páv, Ondřej $u Department of Bioorganic and Medicinal Chemistry, Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
700    1_
$a Rosenberg, Ivan $u Department of Bioorganic and Medicinal Chemistry, Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
773    0_
$w MED00193725 $t Current protocols in nucleic acid chemistry $x 1934-9289 $g Roč. 70, č. - (2017), s. 4.76.1-4.76.22
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28921496 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180709 $b ABA008
991    __
$a 20180712092947 $b ABA008
999    __
$a ok $b bmc $g 1316769 $s 1021559
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 70 $c - $d 4.76.1-4.76.22 $e 20170918 $i 1934-9289 $m Current protocols in nucleic acid chemistry $n Curr Protoc Nucleic Acid Chem $x MED00193725
LZP    __
$a Pubmed-20180709

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...