
Tetrahedron p. 15555 - 15566 (1998)
Update date:2022-09-26
Topics: 1,4-addition Asymmetric Intramolecular Spirocyclization
Yamada, Satoshi
Karasawa, Satoru
Takahashi, Youichi
Aso, Mariko
Suemune, Hiroshi
Novel spirocyclization based on intramolecular 1,4-addition and its asymmetric version have been developed using a combination of Lewis acid and 1,2-diol. Treatment of five- and six-membered α,β-unsaturated cyclic ketones having a 4-oxopentyl group at the
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Doi:10.1016/j.bmcl.2004.03.108
(2004)Doi:10.1055/s-1996-4391
(1996)Doi:10.1055/s-2005-863714
(2005)Doi:10.1016/j.steroids.2003.11.002
(2004)Doi:10.1016/0022-328X(83)85075-X
(1983)Doi:10.1021/ol901597d
(2009)