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Hemi-orthothioamide

Kaloustian and co-workers (37) have reported that the kinetic breakdown of hemi-orthothioamide tetrahedral intermediates (156) was found to involve the preferential cleavage of the C-N bond ( H>8) rather than the C-0 bond (->157). The intermediate J56 were produced in situ by the reaction of sodium hydrosulfide on an imidate salt (J55) in acetone. [Pg.80]

Halogenation of ketones, 275 Hemi-orthoester, 63 Hemi-orthoamide, 103-105 Hemi-orthothioamide, 144 Hemi-orthothiol esters, 93-97 Hinesol, 250... [Pg.195]

See other pages where Hemi-orthothioamide is mentioned: [Pg.80]    [Pg.144]    [Pg.80]    [Pg.144]   
See also in sourсe #XX -- [ Pg.144 ]



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