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Thiophosphoryl tribromide

While technically not "organometallics," enamines are reagents that can provide nucleophilic carbon for new bond formation. Two groups of researchers have reported on the use of such reagents for the formation of new carbon-phosphorus bonds through displacement of chloride from phosphorus.72 73 For example, displacement of bromide from phosphorus tribromide has been used for the introduction of a new thiophosphoryl functionality adjacent to an original carbonyl group (Equation 4.28).72 This approach provides a facile access to (3-ketophosphonates. [Pg.124]


See other pages where Thiophosphoryl tribromide is mentioned: [Pg.267]    [Pg.536]    [Pg.1078]    [Pg.153]    [Pg.267]    [Pg.536]    [Pg.1078]    [Pg.153]    [Pg.1821]    [Pg.220]    [Pg.1024]    [Pg.1032]    [Pg.1033]    [Pg.1035]    [Pg.1036]    [Pg.1052]    [Pg.1076]    [Pg.1077]    [Pg.1077]    [Pg.1907]    [Pg.1821]    [Pg.1153]    [Pg.1239]    [Pg.1821]   
See also in sourсe #XX -- [ Pg.2 , Pg.153 ]




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Phosphorus (V) Sulfobromide (Thiophosphoryl Tribromide)

Thiophosphoryl

Thiophosphorylation

Thiophosphorylations

Tribromide

Tribromides

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