About: Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage.

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About: Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. Goto Sponge NotDistinct Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

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rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	In contrast to O -acetyl group, the O -methoxycarbonyl protecting group was found to be excellent non-participating group for the protection of hydroxy function of derivatives of nucleosides at the activation of phosphorus moiety during phosphotriester synthesis of oligonucleotides. In contrast to O -acetyl group, the O -methoxycarbonyl protecting group was found to be excellent non-participating group for the protection of hydroxy function of derivatives of nucleosides at the activation of phosphorus moiety during phosphotriester synthesis of oligonucleotides. (en)
Title	Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. (en)
skos:prefLabel	Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. Study on reactivity and protection of the .alfa.-hydroxyphosphonate Moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. (en)
skos:notation	RIV/61388963:_____/03:57030116!RIV/2004/GA0/A57004/N
http://linked.open.../vavai/riv/strany	329;347
http://linked.open...avai/riv/aktivita	P Z
http://linked.open...avai/riv/aktivity	P(GA203/01/1166), P(IAA4055101), Z(AV0Z4055905)
http://linked.open...iv/cisloPeriodika	N/A
http://linked.open...vai/riv/dodaniDat	2004
http://linked.open...aciTvurceVysledku	Rosenberg, Ivan Buděšínský, Miloš Králíková, Šárka Masojídková, Milena
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Ústav organické chemie a biochemie AV ČR, v. v. i.
http://linked.open...dnocenehoVysledku	629631
http://linked.open...ai/riv/idVysledku	RIV/61388963:_____/03:57030116
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	protection; .alfa.-hydroxyphosphonates; oligonucleotides (en)
http://linked.open.../riv/klicoveSlovo	protection oligonucleotides .alfa.-hydroxyphosphonates
http://linked.open...odStatuVydavatele	US - Spojené státy americké
http://linked.open...ontrolniKodProRIV	[37E4C9FE86DF]
http://linked.open...i/riv/nazevZdroje	Nucleosides, Nucleotides & Nucleic Acids
http://linked.open...in/vavai/riv/obor	CC
http://linked.open...ichTvurcuVysledku	4 (xsd:int)
http://linked.open...cetTvurcuVysledku	4 (xsd:int)
http://linked.open...ocetUcastnikuAkce	0 (xsd:int)
http://linked.open...nichUcastnikuAkce	0 (xsd:int)
http://linked.open...vavai/riv/projekt	Novel oligonucleotides containing nonisosteric, enzyme-stable phosphonate linkages : systematic physico-chemical study on structure variants Phosphonate-based 2'-5' oligoadenylate analogs: a novel metabolically stable potential activators of RNase L.
http://linked.open...UplatneniVysledku	2003
http://linked.open...v/svazekPeriodika	22
http://linked.open...iv/tvurceVysledku	Buděšínský, Miloš Rosenberg, Ivan Králíková, Šárka Masojídková, Milena
http://linked.open...n/vavai/riv/zamer	Chemical principles of selected biological phenomena in medicine and ecology
issn	1525-7770
number of pages	18 (xsd:int)

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