Synthesis of Nonadeca- and Octadecaribonucleotides Using the Solid-Phase Phosphotriester with Tetrahydropyranyl Groups as the 2′-Hydroxyl-Protecting Group-Reference-Cited by-同舟云学术

Synthesis of Nonadeca- and Octadecaribonucleotides Using the Solid-Phase Phosphotriester with Tetrahydropyranyl Groups as the 2′-Hydroxyl-Protecting Group

Published:1989-06 Issue:6 Volume:62 Page:1995-2001
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Hirao Ichiro,Ishikawa Masahide,Hori Hiroyuki,Watanabe Kimitsuna,Miura Kin-ichiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/62/6/62_6_1995/_pdf

Reference29 articles.

1. Large scale bench-top synthesis of a nineteen unit ribonucleotide on silica gel.

2. Preparation of ribonucleoside 3′-O-phosphoramidites and their application to the automated solid phase synthesis of oligonucleotides

3. Solid phase synthesis of oligoribonucleotides using o-nitrobenzyl protection of 2′-hydroxyl via a phosphite triester approach

4. The automated chemical synthesis of long oligoribuncleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmethionine tRNA

5. Solid phase synthesis of the 3′-terminal nonadecaribonucleoside octadecaphosphate sequence of yeast alanine transfer ribonucleic acid

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