| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223664 | Tetrahedron | 2010 | 12 Pages |
Abstract
The union of functionalized pyrroloindolizines for the synthesis of heterodimeric products relevant to myrmicarin alkaloids is described. Design and synthesis of tricyclic substrates and new methods for their union enable the investigation of late-stage cyclopentannulation strategies. The rapid assembly of dimeric structures using unique modes of pyrroloindolizine reactivity presents a concise approach to the dimeric myrmicarins and relevant derivatives.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alison E. Ondrus, H. Ãmit Kaniskan, Mohammad Movassaghi,