Synthesis of a new enantiomerically pure constrained homoserine
The use of the Diels-Alder reaction between 1,3-butadiene and chiral 2-acetamidoacrylates as the key step followed by stereocontrolled transformations allows the synthesis of (1S,3R)-1-amino-3-hydroxycyclohexanecarboxylic acid, a new type of constrained homoserine, with an excellent overall yield.
| Autores: | , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 1996 |
| País: | España |
| Institución: | Universidad de La Rioja (UR) |
| Repositorio: | RIUR. Repositorio Institucional de la Universidad de La Rioja |
| OAI Identifier: | oai:portal.dialnet.es:doc/5bbc68feb750603269e81311 |
| Acceso en línea: | https://investigacion.unirioja.es/documentos/5bbc68feb750603269e81311 |
| Access Level: | acceso abierto |
| Sumario: | The use of the Diels-Alder reaction between 1,3-butadiene and chiral 2-acetamidoacrylates as the key step followed by stereocontrolled transformations allows the synthesis of (1S,3R)-1-amino-3-hydroxycyclohexanecarboxylic acid, a new type of constrained homoserine, with an excellent overall yield. |
|---|