Synthesis and Reactions of 2,6-Diphenyl-4-(trimethylsilyl)-4H-thiopyran
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.
Chen, Chin H.,Doney, Jeffrey J.,Reynolds, George A.
p. 680 - 684
(2007/10/02)
Synthesis and Reactions of (4H- and 2H-2,6-Diphenylthiopyran-4-yl)phosphonates
The umpolung of 2,6-diphenylthiopyrylium salts is achieved by the synthesis of the Wittig-Horner reagent of diethyl (2,6-diphenyl-4H-thiopyran-4-yl)phosphonate (7).This 4H-lithiated species is a kinetically controlled product which equilibrates to the mor
Chen, Chin H.,Reynolds, George A.
p. 2453 - 2458
(2007/10/02)
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