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. Author manuscript; available in PMC: 2014 Jun 2.
Published in final edited form as: Nat Chem. 2013 May 19;5(6):510–517. doi: 10.1038/nchem.1653

Table 1.

Simultaneous arming/SAR studies of natural products and drugs by amination and aziridination with sulfamate 9.

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a

Diastereomers can be generated with achiral substrates, as in this case with indane, since the sulfamate reagent bears a stereogenic center.

b

C–H amination of dextromethorphan•HBr monohydrate was performed in the presence of K2CO3 (6.0 equiv). (rec. SM = recovered starting material)