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The oxime rearrangement cyclization. Alkenyl, styryl and vinyl chloride terminators in the synthesis of Δ1-pyrrolines

✍ Scribed by Robert E. Gawley; Enrico J. Termine


Book ID
104220316
Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
137 KB
Volume
23
Category
Article
ISSN
0040-4039

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✦ Synopsis


Punctionalized y,6 -unsaturated oximes, constructed by regiospecific alkylation of appropriate oximes, may be rearranged and cyclized to AI-pyrrolines in good yield.

The cationic cyclization of nitrilium ions to form Al-pyrrolines has been known for some time.


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