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Cesar, V., Bellemin-Laponnaz, S., Wadepohl, H. and Gade, L.H. (2005) Designing the “Search Pathway” in the Development of a New Class of Highly Efficient Stereoselective Hydrosilylation Catalysts. Chemistry—A European Journal, 11, 2862-2873.
http://dx.doi.org/10.1002/chem.200500132

has been cited by the following article:

• TITLE: Synthesis and Characterization of New Chiral Monoanionic [ON] Ancillary Phenolate Ligands

  AUTHORS: Pascal Binda, Leslie Glover

  KEYWORDS: Phenolate Ligands, Mannich Condensation Reaction, Ring-Opening Polymerization of Lactones

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.4 No.3, September 11, 2014

  ABSTRACT: Three new chiral monoanionic [ON] ancillary phenolate ligands with varying pendant arms have been synthesized in moderate to high yields (50% - 85%) via Mannich-type condensation reaction of chiral substituted phenol, formaldehyde and (+)-bis-[(R)-1-phenylethyl]amine. These new organic compounds were fully characterized via nuclear magnetic resonance spectroscopy (1H and 13C) and elemental analysis. The newly synthesized ligands are suitable candidates for metal-catalyzed ring-opening of lactones and asymmetric catalysis.