1354558-60-3

Upstream product

• 344313-81-1 7-phenylindan-1-ol 
• 1354558-57-8 N₁,N₂-bis((1R,2R)-2-hydroxy-7-phenyl-2,3-dihydro-1H-inden-1-yl)oxalamide 
• 1354558-55-6 (1R,2R)-1-amino-7-phenyl-2,3-dihydro-1H-inden-2-ol 
• 1354558-53-4 (1R,2R)-1-azido-7-phenyl-2,3-dihydro-1H-inden-2-ol 
• 1354558-51-2 (1S,2R)-epoxy-7'-phenylindane 
• 324534-56-7 4-phenyl-1H-indene 
• 491-37-2 2,3-dihydro-4H-1-benzopyran-4-one 
• 6968-35-0 7-hydroxy-indan-1-one 
• 868374-23-6 3-oxo-2,3-dihydro-1H-inden-4-yl trifluoromethanesulfonate 

Downstream Products

• 1354558-63-6 (3aR,3'aR,8aS,8'aS)-4,4'-diphenyl-8,8a,8',8'a-tetrahydro-3aH,3'aH-2,2'-biindeno[1,2-d]oxazole 
• 1354558-68-1 C₃₃H₂₅N₂O₂⁽¹⁺⁾*I^(1-) 
• 1354694-98-6 CF₃O₃S^(1-)*C₃₃H₂₅N₂O₂⁽¹⁺⁾ 

Relevant academic research and scientific papers

The design and synthesis of novel IBiox N-heterocyclic carbene ligands derived from substituted amino-indanols

A synthetic route towards a number of novel IBiox N-heterocyclic carbene (NHC) ligands has been developed. The resulting ligands have restricted flexibility and high steric demand. Preliminary studies have shown these ligands to give high levels of asymmetric induction in the copper-free allylic alkylation of cinnamyl bromide.