Literature DB >> 29967912

Modification of oligodeoxynucleotides by on-column Suzuki cross-coupling reactions.

Maria Ejlersen1, Chenguang Lou, Yogesh S Sanghvi, Yitzhak Tor, Jesper Wengel.   

Abstract

The on-column functionalization of oligodeoxynucleotides via base-free Suzuki cross-coupling reactions is reported herein. These cross-coupling reactions were carried out with various boronic acids and either full-length modified oligonucleotides containing one or more 2'-deoxy-5-iodouridine (5IdU) monomer(s) or on oligonucleotide fragments immediately after incorporation of 5IdU. Five different functionalities were coupled to oligonucleotides containing one or three attachment points.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29967912     DOI: 10.1039/c8cc01360h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Acrylamide-dT: a polymerisable nucleoside for DNA incorporation.

Authors:  Francia Allabush; Paula M Mendes; James H R Tucker
Journal:  RSC Adv       Date:  2019-10-03       Impact factor: 4.036

2.  Conjugation of oligonucleotides with activated carbamate reagents prepared by the Ugi reaction for oligonucleotide library synthesis.

Authors:  Ryosuke Kita; Takashi Osawa; Satoshi Obika
Journal:  RSC Chem Biol       Date:  2022-04-19

3.  Solid-phase reactive chromatography (SPRC): a sustainable method for the synthesis of benzimidazol-diphenyl-2-imino-thiazolidine-4-ols (hemiaminals) which are active against lung cancer.

Authors:  V M Bangade; P R Mali; H M Meshram
Journal:  RSC Adv       Date:  2021-01-08       Impact factor: 3.361

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.