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. Author manuscript; available in PMC: 2012 Jun 14.
Published in final edited form as: J Med Chem. 2010 Oct 28;53(20):7356–7364. doi: 10.1021/jm100953c

Scheme 1.

Scheme 1

Synthesis of {(1R,2R,4R)-4-Methyl-1,2-cyclohexanediamine}oxalatoplatinum(II), 3aa

a(i) H2O2/HCOOH, (ii) MsCl/Py, NaN3, (iii) Pd/CaCO3, H2 (3 bar), (iv) l-tartaric acid, (v) K2PtCl4/NaOH (0.25 M), and (vi) AgNO3, potassium oxalate. Structures of 4-ethyl- and 4-t-butyl oxaliplatin derivatives 4 and 5, synthesized as enantiomeric mixtures (all substituents at the cyclohexane ring in equatorial positions).