The synthesis and stereoselective conjug
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Russell J Linderman; Alex Godfrey
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Article
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1986
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Elsevier Science
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French
⚖ 214 KB
a-Alkoxystannane J-was prepared by the method by Still.la Transmetallation with nBuLi in THF at -78'C and addition of the lithio anion to a solution of cyclohexenone produced the unstable 1,2-addition product 2. -GC analysis of the crude product mixture indicated that no 1,4-addition had occurred. C