A convenient protocol is developed for the synthesis of 3 `-N-(fluorenylmethoxycarbonyl)-amino]-5 `-carboxymethyl derivatives of all four natural ribonucleosides from cheap chiral pool compound glucose. Synthesis of fully amide-linked RNA analogues of small oligonucleotides containing, for the first time, all four nucleoside amino acids using standard solid phase Fmoc-chemistry is described. (C) 2014 Elsevier Ltd. All rights reserved
The synthesis of nicotinamide adenine dinucleotide (NAD) analogues in which the ribose unit of the n...
Copyright © 2018, Georg Thieme Verlag. All rights reserved. We describe a short and stereospecific s...
This unit contains four basic protocols describing the synthesis of 5-aminoimidazole-4-carboxamide r...
A convenient protocol is developed for the synthesis of 3 `-N-(fluorenylmethoxycarbonyl)-amino]-5 `-...
This thesis describes approaches towards the synthesis of some carbocyclic analogues of nucleosides ...
By chemically modifying or replacing the backbone of oligonucleotides it is possible to modulate the...
Functionalized oligonucleotides have recently gained increased attention for incorporation in modifi...
Due to the increasing interest in the use of oligonucleotide analogues as antisense and antigene dru...
Herein we describe a class of unconventional nucleosides (methyloxynucleosides) that combine unconve...
Nucleoside analogues constitute almost half of today’s major anticancer and antiviral therapeutics. ...
In this article we describe two solid-phase synthetic routes to obtain a nucleo-oligolysine α-peptid...
Oligonucleotides that contain up to three aminopropyl nucleoside analogues have been synthesized. Di...
Nucleoside analogues are a vital class ofcompounds that are used in the treatment of AIDS and other ...
The solid phase approach for the preparation of cyclic oligodeoxy- and oligo-ribonucleotides was imp...
In studies aimed at improving the automated solid-phase synthesis of RNA, a new protecting group, 4-...
The synthesis of nicotinamide adenine dinucleotide (NAD) analogues in which the ribose unit of the n...
Copyright © 2018, Georg Thieme Verlag. All rights reserved. We describe a short and stereospecific s...
This unit contains four basic protocols describing the synthesis of 5-aminoimidazole-4-carboxamide r...
A convenient protocol is developed for the synthesis of 3 `-N-(fluorenylmethoxycarbonyl)-amino]-5 `-...
This thesis describes approaches towards the synthesis of some carbocyclic analogues of nucleosides ...
By chemically modifying or replacing the backbone of oligonucleotides it is possible to modulate the...
Functionalized oligonucleotides have recently gained increased attention for incorporation in modifi...
Due to the increasing interest in the use of oligonucleotide analogues as antisense and antigene dru...
Herein we describe a class of unconventional nucleosides (methyloxynucleosides) that combine unconve...
Nucleoside analogues constitute almost half of today’s major anticancer and antiviral therapeutics. ...
In this article we describe two solid-phase synthetic routes to obtain a nucleo-oligolysine α-peptid...
Oligonucleotides that contain up to three aminopropyl nucleoside analogues have been synthesized. Di...
Nucleoside analogues are a vital class ofcompounds that are used in the treatment of AIDS and other ...
The solid phase approach for the preparation of cyclic oligodeoxy- and oligo-ribonucleotides was imp...
In studies aimed at improving the automated solid-phase synthesis of RNA, a new protecting group, 4-...
The synthesis of nicotinamide adenine dinucleotide (NAD) analogues in which the ribose unit of the n...
Copyright © 2018, Georg Thieme Verlag. All rights reserved. We describe a short and stereospecific s...
This unit contains four basic protocols describing the synthesis of 5-aminoimidazole-4-carboxamide r...