| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265262 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
A direct route for the synthesis of highly functionalized bicyclo[3.2.0]heptane core containing the bridged lactone with the functionalized C-12 substituent of bielschowskysin is reported. The key step involves a stereoselective Cu (I)-catalyzed [2+2] photocycloaddition of a 1,6-diene embedded in a sugar derivative.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anupam Jana, Sujit Mondal, Md. Firoj Hossain, Subrata Ghosh,
![First Page Preview: Stereocontrolled approach to the highly functionalized bicyclo[3.2.0] heptane core of bielschowskysin through intramolecular Cu(I)-catalyzed [2+2] photocycloaddition Stereocontrolled approach to the highly functionalized bicyclo[3.2.0] heptane core of bielschowskysin through intramolecular Cu(I)-catalyzed [2+2] photocycloaddition](/preview/png/5265262.png)