Nucleoside 3'-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. IV. New method for removal of 2,2,2-trichloroethyl group and 31P NMR as a new tool for analysis of deblocking of internucleotide phosphate protecting groups.
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Effects of pendant groups at phosphorus on binding properties of d-ApA analoguesChemical synthesis of the 5'-terminal part bearing cap structure of messenger RNA of cytoplasmic polyhedrosis virus (CPV): m7G5'pppAmpG and m7G5'pppAmpGpU.Studies on the synthesis of nucleotidyl-peptides. II. The preparation of a nucleotidyl-peptide having a 5'-nucleotidyl-(P-O)-serine phosphodiester bond.Tendencies of 31P chemical shifts changes in NMR spectra of nucleotide derivatives.Chromatography on Sephadex LH20 as an efficient purification step after removal of internucleotide 2,2,2-trichloroethyl protective groups from oligoribonucleotide phosphotriesters.The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1.
P2860
Nucleoside 3'-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. IV. New method for removal of 2,2,2-trichloroethyl group and 31P NMR as a new tool for analysis of deblocking of internucleotide phosphate protecting groups.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
1977年论文
@zh
1977年论文
@zh-cn
name
Nucleoside 3'-phosphotriesters ...... e phosphate protecting groups.
@en
type
label
Nucleoside 3'-phosphotriesters ...... e phosphate protecting groups.
@en
prefLabel
Nucleoside 3'-phosphotriesters ...... e phosphate protecting groups.
@en
P2093
P2860
P356
P1476
Nucleoside 3'-phosphotriesters ...... e phosphate protecting groups.
@en
P2093
Grześkowiak
Kraszewski A
Markiewicz WT
Stawiński J
Wiewiórowski
P2860
P304
P356
10.1093/NAR/4.7.2321
P577
1977-07-01T00:00:00Z