Encyclopedia of Reagents for Organic Synthesis 2003
DOI: 10.1002/047084289x.rn00294
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Bis(cyclopentadienyl)titanium(III) Chloride

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Cited by 3 publications
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“…Ti­(III) metalloradicals are powerful intermediates in synthetic chemistry. The radical ring-opening of epoxides is one of their archetypal transformation, as exemplified by the extensive utilization of titanocene­(III) chloride (Cp 2 TiCl, Cp = cyclopentadienyl) in synthesis. These species are also efficient at abstracting halogen-atoms, and while their application in XAT-based transformations is largely based on thermal manifolds requiring stoichiometric reductants (e.g., Zn or Mn), applications in photochemistry and photocatalysis are receiving an increasing attention. …”
Section: Applications Of Xat Reactivity In Synthetic Photocatalysismentioning
confidence: 99%
“…Ti­(III) metalloradicals are powerful intermediates in synthetic chemistry. The radical ring-opening of epoxides is one of their archetypal transformation, as exemplified by the extensive utilization of titanocene­(III) chloride (Cp 2 TiCl, Cp = cyclopentadienyl) in synthesis. These species are also efficient at abstracting halogen-atoms, and while their application in XAT-based transformations is largely based on thermal manifolds requiring stoichiometric reductants (e.g., Zn or Mn), applications in photochemistry and photocatalysis are receiving an increasing attention. …”
Section: Applications Of Xat Reactivity In Synthetic Photocatalysismentioning
confidence: 99%
“…Reactions involving transformations of these compounds to Cp 2 Ti­(III) and Cp 2 Ti­(II) species, loss of the Cp ring, or replacement of halogen by other ligands are also important . The reduction of Cp 2 ­TiCl 2 with Al, Mn, and Zn in tetrahydrofuran (THF) leads to dimeric (Cp 2 ­TiCl) 2 active Nugent’s reagents for highly diastereoselective pinacol coupling reactions of aldehydes, epoxide opening to alkyl radicals, and other reactions . In most organometallic reactions of transition-metal complexes, the η 5 -Cp ligand is a spectator and stays tightly bound to the center throughout the reaction.…”
Section: Introductionmentioning
confidence: 99%
“…Since Tebbe’s reagent is known to exist in various forms in solution, potentially complicating the investigation, we synthesized the simplified analogue bis­(cyclopentadienyl)­titanium chloride (Cp 2 TiCl) to use for comparison. Cp 2 TiCl provides the same {100} shape control as Tebbe’s reagent (Figure S6) and is obtained by a straightforward reduction of Cp 2 TiCl 2 using Al foil. We then compared the catalysts [Me 5 Cp] 2 TiCl 2 and [TbCp] 2 TiCl 2 to Cp 2 TiCl. The catalyst concentration was controllably varied while keeping all other reaction conditions the same.…”
mentioning
confidence: 99%