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Stereoselective Synthesis of the C(1)-C(19) Fragment of Tetrafibricin

[Image: see text] A stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin has been accomplished via a highly diastereoselective double allylboration reaction of 6, 7, and 8, and an iodonium-ion promoted urethane cyclization for the installation of the C(15) alkoxy function in 3.

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Detalhes bibliográficos
Main Authors: Lira, Ricardo, Roush, William R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2701644/
https://ncbi.nlm.nih.gov/pubmed/17249805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol0629869
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