Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
about
Synthesis of DNA via deoxynucleoside H-phosphonate intermediatesThe final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groupsArtificially expanded genetic information system: a new base pair with an alternative hydrogen bonding pattern8-vinyl-deoxyadenosine, an alternative fluorescent nucleoside analog to 2'-deoxyribosyl-2-aminopurine with improved propertiesEnzymatic primer-extension with glycerol-nucleoside triphosphates on DNA templates.Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process.Fluorescent analogs of biomolecular building blocks: design, properties, and applications.A new, but old, nucleoside analog: the first synthesis of 1-deaza-2'-deoxyguanosine and its properties as a nucleoside and as oligodeoxynucleotidesSynthesis and properties of defined DNA oligomers containing base mispairs involving 2-aminopurine.Non-enzymatic DNA cleavage reaction induced by 5-ethynyluracil in methylamine aqueous solution and application to DNA concatenationMicroarray analysis using disiloxyl 70mer oligonucleotides.Strings of contiguous modified pentanucleotides with increased DNA-binding affinity can be used for DNA sequencing by primer walking.DNA synthesis without base protection.A spectroscopic and calorimetric study of the melting behaviors of a "bent" and a "normal" DNA duplex: [d(GA4T4C)]2 versus [d(GT4A4C)]2.ECHO probes: a concept of fluorescence control for practical nucleic acid sensing.Oligodeoxynucleotides containing C-7 propyne analogs of 7-deaza-2'-deoxyguanosine and 7-deaza-2'-deoxyadenosine.Kinetic studies on depurination and detritylation of CPG-bound intermediates during oligonucleotide synthesis.Investigation of the 'n-1' impurity in phosphorothioate oligodeoxynucleotides synthesized by the solid-phase beta-cyanoethyl phosphoramidite method using stepwise sulfurization.Improved synthesis of oligodeoxyribonucleotide using 3-methoxy-4-phenoxybenzoyl group for amino protection.Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH2 and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach.Highly efficient synthesis of oligodeoxyribonucleotides using alpha-phenyl cinnamoyl group for selective amino protection.Cyclic diacyl groups for protection of the N6-amino group of deoxyadenosine in oligodeoxynucleotide synthesisHighly efficient oligodeoxyribonucleotide synthesis using fully base protected phosphodiester building blocks carrying 2-(1-methylimidazol-2-yl) phenyl protection of the phosphate.A new linkage for solid phase synthesis of oligodeoxyribonucleotides.Conformational changes of the phenyl and naphthyl isocyanate-DNA adducts during DNA replication and by minor groove binding molecules.Nucleobase protection of deoxyribo- and ribonucleosides.Synthesis of conformationally locked versions of puromycin analoguesNucleobase Protection of Deoxyribo- and Ribonucleosides.
P2860
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P2860
Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
description
1983 nî lūn-bûn
@nan
1983年の論文
@ja
1983年学术文章
@wuu
1983年学术文章
@zh-cn
1983年学术文章
@zh-hans
1983年学术文章
@zh-my
1983年学术文章
@zh-sg
1983年學術文章
@yue
1983年學術文章
@zh
1983年學術文章
@zh-hant
name
Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
@en
type
label
Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
@en
prefLabel
Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
@en
P2860
P356
P1476
Dialkylformamidines: depurination resistant N6-protecting group for deoxyadenosine.
@en
P2093
Froehler BC
Matteucci MD
P2860
P304
P356
10.1093/NAR/11.22.8031
P577
1983-11-01T00:00:00Z