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- W2000699421 abstract "Abstract The 1,3‐dipolar cycloaddition of an azomethine ylide, generated from isatin and sarcosine by a decarboxylative route with various p‐substituted 3,5 bis(aryl methylidene)N‐methyl‐4‐piperidinones in refluxing methanol, proceeded regioselectively to give novel dispiroheterocycles. The product on subsequent annulation with hydrazine hydrate afforded 1‐N‐methyl‐spiro[2.3′]oxindole‐spiro[3.7″](3″‐aryl)‐5″‐methyl‐3″,3a″,4″,5″,6″,7″‐hexahydro‐2H‐pyrazolo[4,3‐c]pyridine‐4‐aryl‐pyrrolidines in good yield. Keywords: 3,5‐Bis(aryl methylidene)N‐methyl‐4‐piperidinones1,3‐dipolar cycloaddition" @default.
- W2000699421 created "2016-06-24" @default.
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- W2000699421 date "2006-02-01" @default.
- W2000699421 modified "2023-10-16" @default.
- W2000699421 title "Rapid Access for the Synthesis of 1‐N‐Methyl‐spiro[2.3′]oxindole‐spiro[3.7″] (3″‐Aryl)‐5″‐methyl‐3″,3a″,4″,5″,6″,7″‐hexahydro‐2H‐pyrazolo[4,3‐<i>c</i>]pyridine‐4‐aryl‐pyrrolidines Through Sequential 1,3‐Dipolar Cycloaddition and Annulation" @default.
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- W2000699421 doi "https://doi.org/10.1080/00397910500328795" @default.
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