Literature DB >> 23389778

An easy access to fluoroalkanes by deoxygenative hydrofluorination of carbonyl compounds via their tosylhydrazones.

Arvind K Yadav1, Vishnu P Srivastava, Lal Dhar S Yadav.   

Abstract

An efficient and operationally simple synthesis of fluoroalkanes by deoxygenative hydrofluorination of carbonyl compounds via their tosylhydrazone surrogates is reported. The reaction can be carried out in a one-pot procedure directly from carbonyl compounds.

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Year:  2013        PMID： 23389778     DOI： 10.1039/c3cc00122a

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


  4 in total

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Journal:  Science       Date:  2022-02-03       Impact factor: 63.714

2.  Aminofluorination: transition-metal-free N-F bond insertion into diazocarbonyl compounds.

Authors:  Gui Chen; Jinshuai Song; Yinghua Yu; Xuesong Luo; Chunsen Li; Xueliang Huang
Journal:  Chem Sci       Date:  2015-12-14       Impact factor: 9.825

3.  [2 + 2 + 1] Cycloaddition of N-tosylhydrazones, tert-butyl nitrite and alkenes: a general and practical access to isoxazolines.

Authors:  Liang Ma; Feng Jin; Xionglve Cheng; Suyan Tao; Gangzhong Jiang; Xingxing Li; Jinwei Yang; Xiaoguang Bao; Xiaobing Wan
Journal:  Chem Sci       Date:  2021-06-22       Impact factor: 9.825

4.  Trivalent Y3+ ionic sensor development based on (E)-Methyl-N'-nitrobenzylidene-benzenesulfonohydrazide (MNBBSH) derivatives modified with nafion matrix.

Authors:  Mohammad Musarraf Hussain; Mohammed M Rahman; Muhammad Nadeem Arshad; Abdullah M Asiri
Journal:  Sci Rep       Date:  2017-07-19       Impact factor: 4.379
  4 in total

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