Tetrahedron p. 7763 - 7774 (1990)
Update date:2022-07-30
Topics:
Fournet, Guy
Balme, Genevieve
Gore, Jacques
The Heck reaction of alkenes bearing in δ position an enolate of β-diester, βketo ester or β-sulfonyl ester leads to cyclopentanes issued from the intramolecular displacement of the carbone sp3-palladium bond by this enolate. This cyclisation is not observed when the enolate is in β or ε position or in the case of a δ-ethylenic amine and βelimination products are only obtained.
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Doi:10.1021/jo01100a601
(1958)Doi:10.1039/jr9580000120
(1958)Doi:10.1021/jo01066a004
(1961)Doi:10.1002/adsc.201800362
(2018)Doi:10.1039/b714340k
(2008)Doi:10.1021/ja053650h
(2005)
