Reactions of Nitrones with Free Radicals. I. Radical 1,3-Addition to Nitrones
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چکیده
منابع مشابه
Efficient stereoselective nucleophilic addition of pyrroles to chiral nitrones.
Regioselective additions of pyrroles to a variety of optically active nitrones under smooth acidic conditions lead to chiral pyrrolic N-hydroxylamines in good to excellent yields. Depending on the position of the chirality on the nitrone partner, the addition products have been isolated with high diastereoselectivity levels. Reaction of glyoxylate based chiral nitrones either at the C-2 or at t...
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Nitrones are demonstrated to efficiently mediate radical coupling reactions on the example of the conjugation of ATRP-made polymers, yielding macromolecules with distinct functional alkoxyamine centres in mid-chain locations of the chains.
متن کاملReductive Coupling Reactions of Nitrones and Imines, Modern Versions
INTRODUCTION Pinacol coupling was first described by Fittig in 1859, when he reported the formation of 2,3dimethyl-2,3-butanediol (1) from acetone and sodium metal. Since then, this ketyl radical anion coupling process has undergone significant advancement, including the development of asymmetric variants. 3 Alternatives to use of strong reducing metals are low valent transition metals and lant...
متن کاملCan nitrones functionalize carbon nanotubes?
An unprecedented functionalization of multi-walled carbon nanotubes (MWCNTs) has been conveniently achieved by the 1,3-dipolar cycloaddition of a cyclic nitrone. This organic functionalization yields materials with a great solubility in DMF (close to 10 mg per mL of DMF) preferentially occurring at the defects of the MWCNT sp(2) network.
متن کاملTrimethylsilyl chloride promoted synthesis of α-branched amines by nucleophilic addition of organozinc halides to nitrones.
A general procedure for the nucleophilic addition of organozinc halides with nitrones in the presence of trimethylsilyl chloride has been developed. Trimethylsilyl chloride was found to be both an indispensable reaction promoter and a ready hydroxylamine protective agent in these reactions. The produced O-(trimethylsilyl)hydroxylamines can be easily reduced into corresponding amines just by a z...
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1970
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.43.856