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Thietane fused derivatives

Sakamoto et al. also reported the solution photochemistry for la-d, which gave the corresponding thietane-fused -lactams 2a-d as shown in Table 2 [30,31]. For tigloyl derivatives Ic and Id, P-lactams were obtained as a mixture of two stereoisomers (entries 6 and 8). The anti isomers were preferably formed, in ratios of 0.8 and 0.7, respectively. In the solid-state photoreaction of... [Pg.5]

Whereas oxidation leaves the fused thietane derivative 218 intact by giving the corresponding sulfone, reduction produces the 4-isopropyl-l,l-diphenyl-bicyclo[4.1.0]hept-l-ene (219) by extrusion of sulfur (Eq. 58). The general oxidation procedure to convert thietanes to their sulfones comprises refluxing with peracetic acid. [Pg.254]


See other pages where Thietane fused derivatives is mentioned: [Pg.514]    [Pg.514]    [Pg.523]    [Pg.347]    [Pg.221]    [Pg.5]    [Pg.403]    [Pg.404]    [Pg.405]    [Pg.406]    [Pg.408]    [Pg.409]    [Pg.410]    [Pg.411]    [Pg.414]    [Pg.415]    [Pg.416]    [Pg.417]    [Pg.418]    [Pg.419]    [Pg.420]    [Pg.421]    [Pg.422]    [Pg.423]    [Pg.424]    [Pg.425]    [Pg.426]    [Pg.427]    [Pg.428]    [Pg.429]    [Pg.430]    [Pg.431]    [Pg.432]    [Pg.433]    [Pg.434]    [Pg.435]    [Pg.436]    [Pg.437]    [Pg.438]    [Pg.439]    [Pg.440]    [Pg.441]    [Pg.442]    [Pg.443]    [Pg.444]    [Pg.445]   
See also in sourсe #XX -- [ Pg.606 ]




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Thietane

Thietane derivatives

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