Naphthalene-catalysed lithiation of 3-chloro-2-chloromethyl-propene: A barbier-type practical alternative to the trimethylenemethane dianion
摘要:
The reaction of equimolar amounts of 3-chloro-2-chloromethylpropene ( 2 ) and a carbonyl compound ( 3 ) with an excess of lithium powder and a catalytic amount (6%) of naphthalene in tetrahydrofuran at 78°C leads, after hydrolysis with water, to the corresponding diols 4 in a Barbier-type process.
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关键词:
alkylation, arylation, dealkylation, dearylation, C‐acylation, olefination alcohols (acyclic compounds cyclopropane derivatives cyclohexane derivatives polyphenylalkene derivatives (stilbene derivatives
DOI:
10.1002/chin.199243119
被引量:
年份:
1992
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