Proton and carbon resonances in NMR spectra of a number of derivatives of 3β-hydroxy-5α-cholanes, zymosterol synthesis intermediates, have been completely assigned using 2D NMR spectroscopy methods. The stereochemistry of the chiral centers and the structures of the molecules have been confirmed.
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Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 78, No. 2, pp. 207–214, March–April, 2011.
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Baranovsky, A.V., Bolotin, A.A. & Kiselev, V.P. NMR spectra of 3β-hydroxy-5α-cholane derivatives, zymosterol synthesis intermediates. J Appl Spectrosc 78, 189–196 (2011). https://doi.org/10.1007/s10812-011-9445-6
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DOI: https://doi.org/10.1007/s10812-011-9445-6