Literature DB >> 23636417

Synthesis of (E)-nitroolefins via decarboxylative nitration using t-butylnitrite (t-BuONO) and TEMPO.

Srimanta Manna1, Sandipan Jana, Tapish Saboo, Arun Maji, Debabrata Maiti.   

Abstract

Nitroolefins are usually synthesized using the Henry reaction. Here we report an alternative metal-free decarboxylative nitration protocol for the preparation of the nitroolefins from α,β-unsaturated carboxylic acids using t-butylnitrite (t-BuONO) and TEMPO. α,β-Unsaturated carboxylic acids bearing β-aromatic and β-heteroaromatic substituents gave (E)-nitroolefins exclusively under mild conditions. A radical based pathway has been proposed for this decarboxylative nitration reaction.

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Year:  2013        PMID: 23636417     DOI: 10.1039/c3cc41576g

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


  3 in total

1.  1,4-Addition of TMSCCl₃ to nitroalkenes: efficient reaction conditions and mechanistic understanding.

Authors:  Na Wu; Benoit Wahl; Simon Woodward; William Lewis
Journal:  Chemistry       Date:  2014-05-21       Impact factor: 5.236

2.  β-Nitrostyrenes as Potential Anti-leishmanial Agents.

Authors:  Syed Shafi; Farhat Afrin; Mohammad Islamuddin; Garima Chouhan; Intzar Ali; Faatima Naaz; Kalicharan Sharma; Mohammad S Zaman
Journal:  Front Microbiol       Date:  2016-09-01       Impact factor: 5.640

3.  Metal-free, room temperature, acid-K2S2O8 mediated method for the nitration of olefins: an easy approach for the synthesis of nitroolefins.

Authors:  Srinivas Ambala; Rohit Singh; Maninder Singh; Pankaj Singh Cham; Ria Gupta; Gurunadham Munagala; Kushalava Reddy Yempalla; Ram A Vishwakarma; Parvinder Pal Singh
Journal:  RSC Adv       Date:  2019-09-25       Impact factor: 4.036

  3 in total

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