Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Recent developments in sulfone chemistry
2. (a) Dabby, R. E.; Kenyon, J.; Mason, R. F. J. Chem. Soc. 1952, 4881–4882. Similar results are obtained by using magnesium (Lee, G. H.; Lee, H. K. Tetrahedron Lett. 1995, 36, 5607–5608);
3. (b) for other reduction conditions, see: Julia, M.; Uguen, D. Bull. Soc. Chim. Fr. 1976, 513–518.
4. (a) Horner, L.; Neumann, H. Chem. Ber. 1965, 98, 1715–1721. Since a mercury electrode was used, these authors suggest that a tetralkylammonium amalgam is the effective reagent and thus that these electrochemical reductions proceed in the same way as those making use of Na·Hg as the reducing species; the standard potential for sodium amalgam has been estimated to ca. −2 V versus SCE (Mairanovsky, V. G. Angew. Chem. 1976, 283–294);
5. (b) Simonet, J.; Jeminet, G. Bull. Soc. Chim. Fr. 1971, 108, 2754–2760.
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