Synthesis and Consecutive Double Diels-Alder Cycloadditions of 3-Methylene-5-phenylsulfinyl-1-pentene as a Synthetic Equivalent of Parent Cross-conjugated Triene, 3-Methylene-1,4-pentadiene

DOI: 10.1246/cl.1986.1491

Source and publish data:

Chemistry Letters p. 1491 - 1494 (1986)

Update date:2022-08-03

Topics:

Authors:

Wada, Eiji

Nagasaki, Noritaka

Kanemasa, Shuji

Tsuge, Otohiko

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Article abstract of DOI:10.1246/cl.1986.1491

3-Methylene-5-phenylsulfinyl-1-pentene undergoes stepwise double Diels-Alder cycloadditions with two different dienophiles to afford hydronaphthalene skeletons.This sequence corresponds to cross type of diene-transmissive Diels-Alder cycloaddition of pare

Full text of DOI:10.1246/cl.1986.1491

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