
Synthesis p. 79 - 82 (1987)
Update date:2022-07-30
Topics:
Ceruti, Maurizio
Degani, Iacopo
Fochi, Rita
Eleven aldehydes (6a-l) were synthesized by 1-carbon homologation of ketones and aldehydes according to the following sequence: Horner-Emmons reaction of 2-(O,O-dimethylphosphonyl)-1,3-benzodithiole (1) and various carbonyl compounds (2) to give benzo-1,4-dithiafulvenes (3); reduction with sodium borohydride and tetrafluoroboric acid-ether complex in dry acetonitrile to 1,3-benzodithioles (5); subsequent hydrolysis of these with mercury(II)oxide and aqueous tetrafluoroboric acid (35percent) in tetrahydrofuran.The procedure is simple, of wide application, and afforded pure aldehydes in good overall yields (55-88percent).
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Doi:10.1021/ja00256a030
(1987)Doi:10.1016/0008-6215(86)80023-4
(1986)Doi:10.1016/S0040-4020(01)87454-8
(1986)Doi:10.1016/S0040-4039(01)80843-1
(1985)Doi:10.1016/j.bmc.2021.116245
(2021)Doi:10.3390/molecules21091207
(2016)