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Organotitanium reagent

Reetz, M. T. Organotitanium Reagents in Organic Synthesis. A Simple Means to Adjust Reactivity and Selectivity of Carbanions. 106, 1-53 (1982). [Pg.264]

Most successful approaches involving addition reactions in the presence of chiral additives utilize organolithium, organomagnesium and the recently introduced organotitanium reagents, which are known to coordinate with amines, ethers, metal amides and alkoxides. [Pg.147]

M. T. Reetz in Organotitanium Reagents in Organic Synthesis, Springer, Berlin 1986. [Pg.163]

Carbosulfenylation of alkenes. This organotitanium reagent reacts with the trans-p-chloro sulfide 2a, formed by addition of phenylsulfenyl chloride to cyclo-... [Pg.152]

Hughes DL (2004) Applications of Organotitanium Reagents. 6 37-62 Hugl H, Nobis M (2008) Multiphase Catalysis in Industry. 23 1-17... [Pg.197]

Some related organotitanium reagents, e.g., CH3C(OCH3)=C = CHTi[OCH(CH3)2]3, appear to possess high configurational stability, i.e., enantiomer equilibration is slow compared to the rate of reaction with an aldehyde96. [Pg.554]

Reetz M (1986) Organotitanium reagents in organic synthesis, Springer, Berlin Heidelberg New York... [Pg.39]


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Alcohols Organotitanium reagents

Chiral compounds Organotitanium reagents

Organotitanium

Organotitanium reagents reactions with carbonyl compounds

Organotitanium reagents reactivity

Organotitanium reagents synthesis

Titanium Compounds Organotitanium reagents

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