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Statements

Subject Item
n2:RIV%2F61388963%3A_____%2F01%3A57010202%21RIV%2F2003%2FAV0%2FA57003%2FN
rdf:type
n3:Vysledek skos:Concept
dcterms:description
Triphosphate analogues of ( S )-1-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine and ( S )-9-[3-hydroxy-2-(phosphonomethoxy)propyl]adenine (HPMPCpp and HPMPApp) were synthetized via morpholide activated intermediate using 4,4'-dimethoxytrityl (DMTr) group for protection of the 3-hydroxy function. Triphosphate analogues of ( S )-1-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine and ( S )-9-[3-hydroxy-2-(phosphonomethoxy)propyl]adenine (HPMPCpp and HPMPApp) were synthetized via morpholide activated intermediate using 4,4'-dimethoxytrityl (DMTr) group for protection of the 3-hydroxy function.
dcterms:title
An alternative synthesis of HPMPC and HPMPA diphosphoryl derivatives. An alternative synthesis of HPMPC and HPMPA diphosphoryl derivatives.
skos:prefLabel
An alternative synthesis of HPMPC and HPMPA diphosphoryl derivatives. An alternative synthesis of HPMPC and HPMPA diphosphoryl derivatives.
skos:notation
RIV/61388963:_____/01:57010202!RIV/2003/AV0/A57003/N
n4:strany
500;506
n4:aktivita
n12:Z n12:P
n4:aktivity
P(GV203/96/K001), Z(AV0Z4055905)
n4:cisloPeriodika
3
n4:dodaniDat
n5:2003
n4:domaciTvurceVysledku
n7:9587217 n7:9059261 n7:8571325 n7:2758849
n4:druhVysledku
n17:J
n4:duvernostUdaju
n10:S
n4:entitaPredkladatele
n15:predkladatel
n4:idSjednocenehoVysledku
672981
n4:idVysledku
RIV/61388963:_____/01:57010202
n4:jazykVysledku
n18:eng
n4:klicovaSlova
acyclic nucleotide analogs
n4:klicoveSlovo
n14:acyclic%20nucleotide%20analogs
n4:kodStatuVydavatele
CZ - Česká republika
n4:kontrolniKodProRIV
[7EBDB4DB540F]
n4:nazevZdroje
Collection of Czechoslovak Chemical Communications
n4:obor
n8:CC
n4:pocetDomacichTvurcuVysledku
4
n4:pocetTvurcuVysledku
4
n4:pocetUcastnikuAkce
0
n4:pocetZahranicnichUcastnikuAkce
0
n4:projekt
n9:GV203%2F96%2FK001
n4:rokUplatneniVysledku
n5:2001
n4:svazekPeriodika
66
n4:tvurceVysledku
Holý, Antonín Votruba, Ivan Masojídková, Milena Otmar, Miroslav
n4:zamer
n16:AV0Z4055905
s:issn
0010-0765
s:numberOfPages
7