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https://doi.org/10.1016/0040-4039(95)02061-6
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Cite Journal: Tetrahedron Letters |  Publication Date: Dec 1, 1995 |
 Citations: 6 |
Affiliation: Kyoto University
The Michael initialed ketenes, generated in situ from organolithium reagents and α,β-unsaturated BHT esters, were effectively reacted with an anion of trimethyl phosphonoacetate to give conjugated aliene carboxylates having a branched side-chain at C4.
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