Use of the 1-(2-fluorophenyl)-4-methoxypiperidin-4-yl (Fpmp) and related protecting groups in oligoribonucleotide synthesis: stability of internucleotide linkages to aqueous acid-Reference-Cited by-同舟云学术

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Use of the 1-(2-fluorophenyl)-4-methoxypiperidin-4-yl (Fpmp) and related protecting groups in oligoribonucleotide synthesis: stability of internucleotide linkages to aqueous acid

Published:1994 Issue:12 Volume:22 Page:2209-2216
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucl Acids Res

Author:

Capaldi Daniel C.,Reese Colin B.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/22/12/2209/7121421/22-12-2209.pdf

Cited by 54 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Use of Arabinonucleosides for Development and Implementation of a Novel 2′‐ O ‐Protecting Group for Efficient Solid‐Phase Synthesis and 2′‐ O ‐Deprotection of RNA Sequences;Current Protocols;2022-01

2. Synthesis of Nucleobase-Modified RNA Oligonucleotides by Post-Synthetic Approach;Molecules;2020-07-23

3. Recent Development of Chemical Synthesis of RNA;Synthesis of Therapeutic Oligonucleotides;2018

4. The first structurally analysed nucleic acid building block containing the Reese protecting group: 2′-O-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl]-β-D-(1′R,2′R,3′R,4′R)-uridine;Acta Crystallographica Section C Structural Chemistry;2015-04-15

5. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols;Greene's Protective Groups in Organic Synthesis;2014-08-11

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