Reaction Site Diversity in the Reactions of Titanium Hydrazides with Organic Nitriles, Isonitriles and Isocyanates: Ti==N(α) Cycloaddition, Ti==N(α) Insertion and N(α)--N(β) Bond Cleavage.

Eitemau Tebyg

• Reaction site diversity in the reactions of titanium hydrazides with organic nitriles, isonitriles and isocyanates: Ti=N(α) cycloaddition, Ti=N(α) insertion and N(α) -N(β) bond cleavage.
  gan: Schofield, A, et al.
  Cyhoeddwyd: (2011)
• Reactions of Cyclopentadienyl-Amidinate Titanium Hydrazides with CO2, CS2, and Isocyanates: Ti=N-alpha Cycloaddition, Cycloaddition-Insertion, and Cycloaddition-NNR2 Group Transfer Reactions
  gan: Tiong, P, et al.
  Cyhoeddwyd: (2011)
• Site selectivity and reversibility in the reactions of titanium hydrazides with Si-H, Si-X, C-X and H+ reagents: Ti=N(α) 1,2-silane addition, Nβ alkylation, Nα protonation and σ-bond metathesis.
  gan: Tiong, P, et al.
  Cyhoeddwyd: (2012)
• Titanium alkoxyimido (Ti=N-OR) complexes: reductive N-O bond cleavage at the boundary between hydrazide and peroxide ligands.
  gan: Schwarz, A, et al.
  Cyhoeddwyd: (2011)
• Single and double substrate insertion into the Ti=N(alpha) bonds of terminal titanium hydrazides.
  gan: Tiong, P, et al.
  Cyhoeddwyd: (2010)