| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5231734 | Tetrahedron | 2006 | 7 Pages |
Abstract
Thiacalixarene 1,3-bis(hydroxyalkyl)amides selectively cyclize to inherently chiral, doubly capped molecules under the Mitsunobu protocol. Self-condensation on the carboxamide groups to afford O,N-heterocycles was not observed.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Chemoselective ring closure of thiacalix[4]arene-1,3-bis(N-Ï-hydroxyalkylamides) via the Mitsunobu reaction](/preview/png/5231734.png "First Page Preview: Chemoselective ring closure of thiacalix[4]arene-1,3-bis(N-Ï-hydroxyalkylamides) via the Mitsunobu reaction")
Authors
Viktor Csokai, András Simon, Barbara Balázs, Gábor Tóth, István Bitter,