| Literature DB >> 23636417 |
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.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23636417 DOI: 10.1039/c3cc41576g
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222