51829-03-9Relevant academic research and scientific papers
Nature of the lowest electron transitions in the linear conjugated systems derivatives of 2,6-diphenylthiapyrylium: Cationic trimethinecyanine, neutral ethylene, its dication and cation-radical
Kudinova,Melnyk,Kachkovsky,Tolmachev
experimental part, p. 59 - 65 (2012/03/22)
A series of linear conjugated systems of different types containing the 2,6-diphenylthiapyrylium residues as terminal groups have been synthesized and investigated by the combined spectral and quantum-chemical methods. The analysis of calculated by ab ini
Synthesis and Reactions of 2,6-Diphenyl-4-(trimethylsilyl)-4H-thiopyran
Chen, Chin H.,Doney, Jeffrey J.,Reynolds, George A.
, p. 680 - 684 (2007/10/02)
The title compound 3 was synthesized by trimethylsilyl chloride quenching of 2,6-diphenyl-4-lithio-4H-thiopyran (7), which was obtained by direct lithiation (n-BuLi) of either the 4H-thiopyran 10 or the 2H isomer 6.Compound 6 was readily prepared in one step from the reaction of 2,6-diphenyl-4-hydroxy-4H-thiopyran (5) with NCS in 74percent yield.Compound 3 was metalated to give 12 in 80-85percent yield by using a combination of n-BuLi and t-BuOK in THF at an internal temperature slightly below -20 deg C.The successful reaction of 12 with a variety of ketones and aldehydes provides an alternative synthesis of the Δ4-2,6-diphenyl-4H-thiopyrans 16.The scope and limitation of this Peterson-type reaction of 12 is compared with those of the corresponding Wittig-Horner reagent 2.
