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Selectivities in the Reactions of Alkyl‐, Aryl‐ and Heterosubstituted Organotitanium Compounds Preliminary Communication
90
Citations
13
References
1981
Year
Organotitanium CompoundsChemical EngineeringEngineeringHeterocyclicTable 3Organic ChemistryOrganometallic CatalysisChemistrySelective CarbonylophilesHeterocycle ChemistryInorganic Synthesis
Abstract Solutions of the title compounds R‐Ti(OR′) 3 ( 1 ) are generally available from organolithium (or magnesium) derivatives according to equation 1. It is shown ( Table 1 ) that some heterosubstituted organotitanium compounds are more stable thermally than their lithium counterparts. The reagents 1 are highly selective carbonylophiles ( Tables 1 and 2 ), their reactivity can be modified by variation of the R′O‐group ( Table 3 ) and with the chiral ( S )‐2‐methyl‐l‐butoxy group an enantioselective addition can be achieved [equ. 2].
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