Asymmetric hetero Diels-Alder as an access to carbacephams
A short and efficient asymmetric synthesis of the (6R,7S)-7-tert-butoxycarbonylamino-2-ketocarbacepham is described. The key step involves the hetero Diels-Alder reaction of the benzylimine derived from the enantiomer of Garner's aldehyde with Danishefsky's diene.
Detalhes bibliográficos
| Autores: |
Avenoza, A. [0000-0002-5465-3555],
Busto, J.H. [0000-0003-4403-4790],
Cativiela, C.,
Corzana, F. [0000-0001-5597-8127],
Peregrina, J.M. [0000-0003-3778-7065],
Zurbano, M.M. [0000-0001-6370-3537] |
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| Tipo de documento: | artigo
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| Estado: | Versão publicada |
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| Data de publicação: | 2002 |
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| País: | España |
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| Recursos: | Universidad de La Rioja (UR) |
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| Repositório: | RIUR. Repositorio Institucional de la Universidad de La Rioja |
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| OAI Identifier: | oai:portal.dialnet.es:doc/5bbc6905b750603269e8139e |
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| Acesso em linha: | https://investigacion.unirioja.es/documentos/5bbc6905b750603269e8139e
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| Access Level: | Acceso aberto |
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