Hydroxycyclopentanone derivatives from D-Mannose via ring closing metathesis: An improved synthesis of a key intermediate of Tricyclo-DNA
| Data(s) |
2003
|
|---|---|
| Resumo |
A large scale, 10 step synthesis of cyclopentanone 1 , starting from the chiral pool compound D-mannose, is described. The synthesis proceeds via a ring closing metathesis reaction as the key step in an overall yield of 23%. Cyclopentanone 1 is a central intermediate for the synthesis of tricyclo-DNA |
| Formato |
application/pdf |
| Identificador |
http://boris.unibe.ch/68561/8/s-2003-39177.pdf Vonlanthen, David; Leumann, Christian (2003). Hydroxycyclopentanone derivatives from D-Mannose via ring closing metathesis: An improved synthesis of a key intermediate of Tricyclo-DNA. Synthesis - journal of synthetic organic chemistry, 2003(07), pp. 1087-1090. Thieme 10.1055/s-2003-39177 <http://dx.doi.org/10.1055/s-2003-39177> doi:10.7892/boris.68561 info:doi:10.1055/s-2003-39177 urn:issn:0039-7881 |
| Idioma(s) |
eng |
| Publicador |
Thieme |
| Relação |
http://boris.unibe.ch/68561/ |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
Vonlanthen, David; Leumann, Christian (2003). Hydroxycyclopentanone derivatives from D-Mannose via ring closing metathesis: An improved synthesis of a key intermediate of Tricyclo-DNA. Synthesis - journal of synthetic organic chemistry, 2003(07), pp. 1087-1090. Thieme 10.1055/s-2003-39177 <http://dx.doi.org/10.1055/s-2003-39177> |
| Palavras-Chave | #570 Life sciences; biology #540 Chemistry |
| Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |
