Asymmetric synthesis of nonracemic primary amines via spiroborate-catalyzed reduction of pure (E)- and (Z)-O-benzyloximes: applications toward the synthesis of calcimimetic agents.

Highly enantiopure (1-aryl)- and (1-naphthyl)-1-ethylamines were synthesized by the borane-mediated reduction of single-isomeric (E)- and (Z)-O-benzyloxime ethers using the stable spiroborate ester derived from (S)-diphenyl valinol and ethylene glycol as the chiral catalyst. Primary (R)-arylethylamines were prepared by the reduction of pure (Z)-ethanone oxime ethers in up to 99% ee using 15% of catalyst. Two convenient and facile approaches to the synthesis of new and known calcimimetic analogues employing enantiopure (1-naphthalen-1-yl)ethylamine as chiral precursor are described.

Development of a quantitative assay to measure EBV viral load in patients with autoimmune type 1 diabetes and healthy subjects.

Clinical studies of immune modulating agents such as otelixizumab, an anti-CD3 monoclonal antibody that is being investigated as a possible treatment for type 1 diabetes, required a sensitive, specific, reproducible method of quantifying Epstein-Barr virus (EBV) load in healthy adults and in patients with conditions not generally associated with increased EBV levels. An assay was developed using a commercial kit and was fully validated. To enhance assay sensitivity and reproducibility, viral load was quantified per 10(6) peripheral blood mononuclear cells (PBMCs) rather than per ml blood.