Journal of Organic Chemistry p. 4326 - 4329 (1983)
Update date:2022-08-02
Topics:
Sawhney, Kailash N.
Lemke, Thomas L.
Schiff base formation has been shown to occur preferentially at the exocyclic carbonyl of 2-acyl-1,3-indandiones (1).The resulting addition product exists either as an open-chain compound (10-16) or as a cyclic hemiketal (19-27).The size of the acyl subst
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Doi:10.1016/j.bmc.2014.09.008
(2014)Doi:10.1016/j.ejmech.2005.07.004
(2005)Doi:10.1016/S0040-4039(00)81677-9
(1983)Doi:10.1016/S0040-4039(00)81938-3
(1983)Doi:10.1021/jo0515475
(2005)Doi:10.1002/ejoc.200500381
(2005)
