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During optimization trials, we noticed unexpectedly the formation of the (20E)-sulfonylimine derivative 2a when (S)-(-)-2-methyl-2-propanesulfinamide was used in excess to the steroidal ketone. The structure of 2a was verified by X-ray analysis. For spectroscopic data of 2a see Supplementary data
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During optimization trials, we noticed unexpectedly the formation of the (20E)-sulfonylimine derivative 2a when (S)-(-)-2-methyl-2-propanesulfinamide was used in excess to the steroidal ketone. The structure of 2a was verified by X-ray analysis. For spectroscopic data of 2a see Supplementary data.
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In the case of imine 13 excess of the chiral auxiliary was necessary for the complete consumption of the steroidal ketone 2
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In the case of imine 13 excess of the chiral auxiliary was necessary for the complete consumption of the steroidal ketone 2.
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CCDC-753934, 753933, 753936, 753935 and 753937 (2, 2a, 4, 13 and 15, respectively) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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