Literature DB >> 33425033

An atom-economical addition of methyl azaarenes with aromatic aldehydes via benzylic C(sp3)-H bond functionalization under solvent- and catalyst-free conditions.

Divya Rohini Yennamaneni1,2, Vasu Amrutham1,2, Krishna Sai Gajula1,2, Rammurthy Banothu1,2, Murali Boosa1,2, Narender Nama1,2.   

Abstract

A convenient practical approach for the synthesis of 2-(pyridin-2-yl)ethanols by direct benzylic addition of azaarenes and aldehydes under catalyst- and solvent-free conditions is reported. This reaction is metal-free, green, and was carried out in a facile operative environment without using any hazardous transition metal catalysts or any other coupling reagents. Different aromatic aldehydes and azaarenes were monitored, and the yields of the resulting products were moderate to excellent. We accomplished several azaarene derivatives under neat conditions through a highly atom-economical pathway. To evaluate the preparative potential of this process, gram-scale reactions were performed up to a 10 g scale.
Copyright © 2020, Yennamaneni et al.; licensee Beilstein-Institut.

Entities:  

Keywords:  aldehydes; azaarenes; benzylic addition; green chemistry; solvent-free conditions

Year:  2020        PMID: 33425033      PMCID: PMC7770386          DOI: 10.3762/bjoc.16.259

Source DB:  PubMed          Journal:  Beilstein J Org Chem        ISSN: 1860-5397            Impact factor:   2.883


  25 in total

1.  Catalytic coupling of C-H and C-I bonds using pyridine as a directing group.

Authors:  Dmitry Shabashov; Olafs Daugulis
Journal:  Org Lett       Date:  2005-08-18       Impact factor: 6.005

2.  Nickel-catalyzed addition of pyridine-N-oxides across alkynes.

Authors:  Kyalo Stephen Kanyiva; Yoshiaki Nakao; Tamejiro Hiyama
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

3.  Functionalization of organic molecules by transition-metal-catalyzed C(sp3)-H activation.

Authors:  Rodolphe Jazzar; Julien Hitce; Alice Renaudat; Julien Sofack-Kreutzer; Olivier Baudoin
Journal:  Chemistry       Date:  2010-03-01       Impact factor: 5.236

4.  Nickel-catalyzed reaction of arylzinc reagents with N-aromatic heterocycles: a straightforward approach to C-H bond arylation of electron-deficient heteroaromatic compounds.

Authors:  Mamoru Tobisu; Isao Hyodo; Naoto Chatani
Journal:  J Am Chem Soc       Date:  2009-09-02       Impact factor: 15.419

5.  Activity against Mycobacterium tuberculosis of alkaloid constituents of Angostura bark, Galipea officinalis.

Authors:  P J Houghton; T Z Woldemariam; Y Watanabe; M Yates
Journal:  Planta Med       Date:  1999-04       Impact factor: 3.352

6.  Palladium-catalyzed benzylic addition of 2-methyl azaarenes to N-sulfonyl aldimines via C-H bond activation.

Authors:  Bo Qian; Shengmei Guo; Jianping Shao; Qiming Zhu; Lei Yang; Chungu Xia; Hanmin Huang
Journal:  J Am Chem Soc       Date:  2010-03-24       Impact factor: 15.419

7.  2,5-Disubstituted pyridines: the discovery of a novel series of 5-HT2A ligands.

Authors:  Kevin J Wilson; Monique B van Niel; Laura Cooper; Dawn Bloomfield; Desmond O'Connor; L Rebecca Fish; Angus M MacLeod
Journal:  Bioorg Med Chem Lett       Date:  2007-02-02       Impact factor: 2.823

8.  Iron-catalyzed direct alkenylation of 2-substituted azaarenes with N-sulfonyl aldimines via C-H bond activation.

Authors:  Bo Qian; Pan Xie; Yinjun Xie; Hanmin Huang
Journal:  Org Lett       Date:  2011-04-29       Impact factor: 6.005

9.  2-Pyridinyl-3-(4-methylsulfonyl)phenylpyridines: selective and orally active cyclooxygenase-2 inhibitors.

Authors:  R W Friesen; C Brideau; C C Chan; S Charleson; D Deschênes; D Dubé; D Ethier; R Fortin; J Y Gauthier; Y Girard; R Gordon; G M Greig; D Riendeau; C Savoie; Z Wang; E Wong; D Visco; L J Xu; R N Young
Journal:  Bioorg Med Chem Lett       Date:  1998-10-06       Impact factor: 2.823

10.  Palladium-catalyzed alkenylation of quinoline-N-oxides via C-H activation under external-oxidant-free conditions.

Authors:  Junliang Wu; Xiuling Cui; Lianmei Chen; Guojie Jiang; Yangjie Wu
Journal:  J Am Chem Soc       Date:  2009-10-07       Impact factor: 15.419

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