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• Marco Caricato, Carmine Coluccini, Daniele Dondi, Douglas A. Vander Griend and Dario Pasini. Nesting complexation of C with large, rigid D symmetrical macrocycles, Org. Biomol. Chem., 2010, 8, 3272.

  [DOI: 10.1039/c004379f]
  
• Carmine Coluccini, Andrea Mazzanti and Dario Pasini. Locked chromophores as CD and NMR probes for the helical conformation of tetraamidic macrocycles, Org. Biomol. Chem., 2010, 8, 1807.

  [DOI: 10.1039/b924400j]
  
• Fernández-Ibáñez M. Ángeles. Catalytic enantioselective Reformatsky reaction with ketones, Chemical Communications, 2008

  [DOI: 10.1039/b801749b]
  
• Barry M. Trost and Cheyenne S. Brindle. The direct catalytic asymmetric aldol reaction, Chem. Soc. Rev., 2010, 39, 1600.

  [DOI: 10.1039/b923537j]
  
• Takizawa Shinobu. Chiral dinuclear vanadium(v) catalysts for oxidative coupling of 2-naphthols, Chemical Communications, 2008

  [DOI: 10.1039/b717068h]
  
• Takizawa Shinobu. Dinuclear chiral vanadium catalysts for oxidative coupling of 2-naphthols via a dual activation mechanism, Chemical Communications, 2008

  [DOI: 10.1039/b806016a]
  
• Carmine Coluccini, Daniele Dondi, Marco Caricato, Angelo Taglietti, Massimo Boiocchi and Dario Pasini. Structurally-variable, rigid and optically-active D and D macrocycles possessing recognition properties towards C, Org. Biomol. Chem., 2010, 8, 1640.

  [DOI: 10.1039/b920867d]
  
• Prabhakar Bachu and Takahiko Akiyama. Enantioselective Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated acyl phosphonates catalyzed by chiral phosphoric acid, Chem. Commun., 2010, 46, 4112.

  [DOI: 10.1039/c000862a]
  
• Xiao-Qing Wu, Qing-Chun Huang, Xiao-Zhen Chen, Guo-You Li and Guo-Lin Zhang . (3S,NR)-3-Hydroxymethyl-2-methyl-2-(3-methylbut-2-en-1-yl)-1,2,3,4-tetrahydroisoquinolinium bromide-1,1'-bi-2-naphthol (1/1) , Acta Cryst (2010). E66, o768  

  [DOI: 10.1107/S1600536810007944]
  
• J.-X. Yuan, Z.-L. Shen, L. Li, X.-Y. Song and Z.-M. Jin. Dicyclohexylammonium 1-(2-hydroxy-1-naphthyl)-2-naphtholate, Acta Cryst. (2005). E61, o3712-o3714    

  [DOI: 10.1107/S1600536805032447]