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A facile route to polysubstituted 2-hydroxy-3-nitro-cyclopentanones via a linear α-ketoenamine

✍ Scribed by F. Felluga; P. Nitti; G. Pitacco; E. Valentin

Book ID
104216595
Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
198 KB
Volume
29
Category
Article
ISSN
0040-4039

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✦ Synopsis

The morpholino monoenamine of diacetyl has been synthesized and reacted with conjugated nitroolefins to give functionalized cyclopentanone derivatives, after hydrolysis of the isolated enamine intermediates.

The importance of nitroalkenes in organic synthesis is well known, as underlined in some reviews on this subject.

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