| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273803 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A novel, concise, stereocontrolled approach to nine-membered carbasugar analogues (cyclononitols) from a bicyclo[4.3.1]deca-2,4-dien-10-one scaffold, harbouring a ‘locked’ cyclononane ring and latent functionalities, is described.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
