A comparison of β-functionalized ethyl groups for the protection of the phospho function in decathymidylate synthesis using a phosphite triester approach-Reference-Cited by-同舟云学术

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A comparison of β-functionalized ethyl groups for the protection of the phospho function in decathymidylate synthesis using a phosphite triester approach

Published:2010-09-02 Issue:7-8 Volume:104 Page:209-214
ISSN:0165-0513
Container-title:Recueil des Travaux Chimiques des Pays-Bas
language:en
Short-container-title:Recl. Trav. Chim. Pays-Bas

Author:

Claesen C. A. A.,Segers R. P. A. M.,Tesser G. I.

Publisher

Wiley

Subject

General Chemistry

Reference20 articles.

1. Ar(alk)ylsulfonyl ethyl groups as phosphorus-protecting functions

2. 9-Fluorenylmethoxycarbonyl amino-protecting group

3. A new solid phase approach for rapid syntheses of oligonucleotides bearing a 3′-terminal phosphate group

Cited by 8 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. Efficient Synthesis of α‐P‐Modified Nucleoside Triphosphates and Dinucleoside Tetraphosphates via Linear P^VP^VP^III‐Nucleoside Intermediates;Asian Journal of Organic Chemistry;2023-02-10

2. Protection for the Phosphate Group;Greene's Protective Groups in Organic Synthesis;2014-08-11

3. Experiences in Z-Deprotection. Simple Preparations of Z-His and diz-His;Bulletin des Sociétés Chimiques Belges;2010-09-01

4. (2-Phenylsulfonyl)ethoxy Dichlorophosphine;Encyclopedia of Reagents for Organic Synthesis;2003-10-15

5. Protecting Groups in Oligonucleotide Synthesis;Protocols for Oligonucleotide Conjugates;1994

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