Literature DB >> 20714566

A sequential direct arylation/Suzuki-Miyaura cross-coupling transformation of unprotected 2'-deoxyadenosine affords a novel class of fluorescent analogues.

Thomas E Storr1, Johanna A Strohmeier, Christoph G Baumann, Ian J S Fairlamb.   

Abstract

Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd(0)-coupling approach.

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Year:  2010        PMID： 20714566     DOI： 10.1039/c0cc02043e

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


  3 in total

1.  Mild and Regioselective Pd(OAc)2-Catalyzed C-H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid.

Authors:  Alan J Reay; L Anders Hammarback; Joshua T W Bray; Thomas Sheridan; David Turnbull; Adrian C Whitwood; Ian J S Fairlamb
Journal:  ACS Catal       Date:  2017-07-10       Impact factor: 13.084

2.  Crystal structure of 8-(4-methyl-phen-yl)-2'-de-oxy-adenosine hemihydrate.

Authors:  Ajaykumar V Ardhapure; Yogesh S Sanghvi; Yulia Borozdina; Anant Ramakant Kapdi; Carola Schulzke
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-01-01

3.  Nucleophilic Arylation of Halopurines Facilitated by Brønsted Acid in Fluoroalcohol.

Authors:  Naoko Takenaga; Toshitaka Shoji; Takayuki Menjo; Akiko Hirai; Shohei Ueda; Kotaro Kikushima; Tomonori Hanasaki; Toshifumi Dohi
Journal:  Molecules       Date:  2019-10-23       Impact factor: 4.411
  3 in total

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