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A facile synthesis of ferrocene grafted N-methyl-spiropyrrolidines through 1,3-dipolar cycloaddition of azomethine ylides

✍ Scribed by A.R. Sureshbabu; R. Raghunathan; B.K. Satiskumar


Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
646 KB
Volume
50
Category
Article
ISSN
0040-4039

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✦ Synopsis


One-pot synthesis of novel ferrocene grafted N-methyl-spiropyrrolidines has been accomplished in good yields through a facile 1,3-dipolar cycloaddition reaction of various azomethine ylide derived from ninhydrin and sarcosine with various ferrocene derivatives as dipolarophile. The regiochemical and stereochemical outcome of the cycloaddition reaction is ascertained by X-ray crystallographic studies of one of the cycloadducts.


πŸ“œ SIMILAR VOLUMES


Synthesis of spiropyrrolidines: 1,3-dipo
✍ A. Amal Raj; R. Raghunathan; E. J. P. Malar πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 312 KB πŸ‘ 2 views

A simple and efficient method for the synthesis of novel spiropyrrolidines has been accomplished by regioselective 1,3-dipolar cycloaddition reactions of an azomethine ylide generated by thermalring opening of cis-1-cyclohexyl-2-phenyl-3-benzoyl aziridine with various (E)-3-arylidene-4-chromanones.

1,3-Dipolar cycloaddition of unstabilize
✍ Alexey M. Starosotnikov; Maxim A. Bastrakov; Sergey Yu. Pechenkin; Margarita A. πŸ“‚ Article πŸ“… 2011 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 124 KB

## Abstract The 1,3‐dipolar cycloaddition of unstabilized __N__‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts