| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5282516 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
The 3,5,7-trisubstituted dioxabicyclic portion of cyclodidemniserinol trisulfate was synthesized by employing intramolecular ketal formation strategy via a convergent and a linear stereoselective synthesis approach, respectively.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Studies toward the total synthesis of cyclodidemniserinol trisulfate. Part I: 3,5,7-Trisubstituted 6,8-dioxabicyclo [3.2.1] octane core structure construction via a convergent and a linear stereoselective synthesis](/preview/png/5282516.png "First Page Preview: Studies toward the total synthesis of cyclodidemniserinol trisulfate. Part I: 3,5,7-Trisubstituted 6,8-dioxabicyclo [3.2.1] octane core structure construction via a convergent and a linear stereoselective synthesis")
Authors
Jian-Hua Liu, Lai-Dong Song, Ya-Qiu Long,