Unexpected reaction of α-aryl-N-(β-phenylethyl) nitrones with chlorinating agents

Article abstract of DOI:10.1080/00397919908086190

The α-aryl-N-(β-phenylethyl)nitrones when subjected to SO₂Cl₂/Et₃N and NCS/NaOMe treatment independently, gave unexpectedly the corresponding amides. These procedures form an alternative route for the rearrangement of nitrones to amides.

Full text of DOI:10.1080/00397919908086190

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Unexpected Reaction Of A-
Aryl-N-(P-Phenylethyl) Nitrones
With Chlorinating Agents
Ponnusamy Mohan a , Arumugasamy Vanangamudi
b , Muniappan Thirumalaikumar b , Shanmugam
Muthusubramanian b & Shunmugaperumal
Sivasubramanian a
a Department of Chemistry , The American College ,
Madurai, 625 002, India
b Department of Organic Chemistry , Madurai
Kamaraj University , Madurai, 625 021, India
Published online: 17 Sep 2007.
To cite this article: Ponnusamy Mohan , Arumugasamy Vanangamudi , Muniappan
Thirumalaikumar , Shanmugam Muthusubramanian & Shunmugaperumal
Sivasubramanian (1999) Unexpected Reaction Of A-Aryl-N-(P-Phenylethyl) Nitrones
With Chlorinating Agents, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:11, 2013-2017, DOI:
10.1080/00397919908086190
To link to this article: http://dx.doi.org/10.1080/00397919908086190
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