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Stereoselectivity of Intramolecular S(N)′ Cyclizations of Alkyllithium Reagents on Methoxy Alkenes

The cyclization of alkyllithium reagents onto methoxy alkenes has been investigated. The alkyllithium reagent was generated by reductive lithiation of an alkyl nitrile. In an unbiased substrate, a methoxy leaving group attached to a stereogenic secondary carbon atom led to the cyclization product wi...

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Hlavní autoři: La Cruz, Thomas E., Rychnovsky, Scott D.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2006
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2496923/
https://ncbi.nlm.nih.gov/pubmed/16438522
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo052166u
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