| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271054 | Tetrahedron Letters | 2010 | 7 Pages |
Abstract
Stereocontrolled synthesis of substituted isonitriles from the Baylis-Hillman adducts of acrylates has been developed. Ugi reaction of these isonitriles with TMSN3, aliphatic amines, and aldehydes or ketone affords 1-substituted tetrazoles which have been demonstrated to be suitable substrates for producing tetrazolo-fused diazepinones.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Maloy Nayak, Sanjay Batra,