Abstract
A one-pot protocol for the formation of 2-nitrobenzenesulfo-nylhydrazide (NBSH) from commercial reagents and subsequent alkene reduction is presented. The transformation is operationally simple and generally efficient for effecting diimide alkene reductions. A range of 16 substrates have been reduced, highlighting the unique chemoselectivity of diimide as a reduction system.
Original language | English |
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Pages (from-to) | 3186-3188 |
Number of pages | 3 |
Journal | Journal of Organic Chemistry |
Volume | 74 |
Issue number | 8 |
DOIs | |
Publication status | Published - 17 Apr 2009 |