An article Chemoselective and metal-free reduction of alpha,beta-unsaturated ketones byin situproduced benzeneselenol fromO-(tert-butyl) Se-phenyl selenocarbonate WOS:000571760600010 published article about OXYGEN INDUCED REDUCTION; CARBONYL-COMPOUNDS; ENANTIOSELECTIVE SYNTHESIS; SELECTIVE 1,4-REDUCTION; CONJUGATE REDUCTION; COUPLING REACTIONS; CHALCONES; ALKENES; ALKYLATION; ALDEHYDES in [Temperini, Andrea; Ballarotto, Marco] Univ Perugia, Dipartimento Sci Farmaceut, Consorzio CINMPIS, Via Liceo 1, I-06123 Perugia, Italy; [Siciliano, Carlo] Univ Calabria, Dipartimento Farm & Sci Salute & Nutr, Edificio Polifunz, I-87030 Cosenza, Italy in 2020.0, Cited 59.0. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7. COA of Formula: C9H10O3
The carbon-carbon double bond of arylidene acetones and chalcones can be selectively reduced with benzeneselenol generatedin situby reactingO-(tert-butyl) Se-phenyl selenocarbonate with hydrochloric acid in ethanol. This mild, metal-free and experimentally simple reduction procedure displays considerable functional-group compatibility, products are obtained in good to excellent yields, and the use of toxic Se/CO mixture and NaSeH, or the smelly and air-sensitive benzeneselenol, is avoided.
COA of Formula: C9H10O3. Welcome to talk about 93-02-7, If you have any questions, you can contact Temperini, A; Ballarotto, M; Siciliano, C or send Email.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com