Literature DB >> 17696491

5(6)-carboxyfluorescein revisited: new protecting group, separation of isomers, and their spectral properties on oligonucleotides.

Maksim V Kvach1, Dmitry A Tsybulsky, Alexey V Ustinov, Irina A Stepanova, Stanislav L Bondarev, Sergey V Gontarev, Vladimir A Korshun, Vadim V Shmanai.   

Abstract

Pentafluorophenyl esters of 5- and 6-carboxyfluorescein-3',6'-O-dipivalate can be easily separated in multigram quantities by column chromatography. The individual isomers were converted into stable phosphoramidites suitable for oligonucleotide synthesis. The use of the cyclohexylcarbonyl (Chc) protecting group instead of pivaloyl (Piv) facilitates the separation of isomers. The fluorescence spectra of 5- and 6-carboxyfluoresceins on oligonucleotides were compared.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17696491     DOI: 10.1021/bc7001874

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  3 in total

1.  Separating the isomers--efficient synthesis of the N-hydroxysuccinimide esters of 5 and 6-carboxyfluorescein diacetate and 5 and 6-carboxyrhodamine B.

Authors:  Aurélie Brunet; Tashfeen Aslam; Mark Bradley
Journal:  Bioorg Med Chem Lett       Date:  2014-05-04       Impact factor: 2.823

2.  Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties.

Authors:  Nancy M Okuda-Shinagawa; Yulia E Moskalenko; Helena C Junqueira; Maurício S Baptista; Carlos M Marques; M Terêsa Machini
Journal:  ACS Omega       Date:  2017-11-20

3.  Molecular Beacon DNA Probes with Fluorescein Bifluorophore.

Authors:  V A Brylev; I L Lysenko; E A Kokin; Y V Martynenko-Makaev; D Y Ryazantsev; V V Shmanai; V A Korshun
Journal:  Russ J Bioorg Chem       Date:  2021-06-11       Impact factor: 0.796

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.