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Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides

Attack of cellular thiols on the antitumor natural product leinamycin is believed to generate a sulfenate intermediate that undergoes subsequent rearrangement to a DNA-alkylating episulfonium ion. Here, 2-(trimethylsilyl)ethyl sulfoxides were employed in a fluoride-triggered generation of sulfenate...

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Detalhes bibliográficos
Main Authors: Keerthi, Kripa, Gates, Kent S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2812901/
https://ncbi.nlm.nih.gov/pubmed/17571189
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/b701179b
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