| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270544 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
A one-pot synthesis of ferrocene-grafted dispiropyrrolidine/pyrrolizidine scaffolds has been accomplished in good yields through a facile 1,3-dipolar cycloaddition of various azomethine ylides derived from diketones and secondary amino acids with Baylis-Hillman adduct derived from ferrocene carbaldehyde. The regiochemical and stereochemical outcomes of the cycloaddition reaction were ascertained by X-ray crystallographic studies of one of the cycloadducts.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![A facile one-pot three-component synthesis of ferrocene-grafted dispiro pyrrolidine/pyrrolizidine scaffolds through intermolecular [3+2] cycloaddition reaction of ferrocenyl Baylis-Hillman adduct](/preview/png/5270544.png "First Page Preview: A facile one-pot three-component synthesis of ferrocene-grafted dispiro pyrrolidine/pyrrolizidine scaffolds through intermolecular [3+2] cycloaddition reaction of ferrocenyl Baylis-Hillman adduct")
Authors
Subban Kathiravan, Raghavachary Raghunathan,