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. Author manuscript; available in PMC: 2016 Feb 12.
Published in final edited form as: Inorg Chem. 2015 May 5;54(17):8214–8222. doi: 10.1021/acs.inorgchem.5b00532

Figure 4.

Figure 4

(a) Structures of 1a and 1b highlighting corresponding protons used for integration data from 1H NMR spectra in (b) chloroform-d and (c) acetonitrile-d3; (d) equilibrium between the open form 1a or 2a and the two R and S diastereomers of the pyran forms 1b and 2b; two signals in the 1H NMR spectrum (highlighted in green in acetonitrile-d3) are for H7 in the pyran form, each corresponding to either the R or S isomer.