Theoretical studies on selectivities in the Staudinger reaction of vicinal diimines and ketenes
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s11426-012-4801-9.pdf
Reference50 articles.
1. Georg GI. The Organic Chemistry of β-Lactams. New York: Verlag Chemie, 1992
2. Palomo C, Aizpurua JM, Ganboa I, Oiarbide M. Asymmetric synthesis of β-lactams by Staudinger ketene-imine cycloaddition reaction. Eur J Org Chem, 1999, 3223-3225
3. Singh GS. Recent progress in the synthesis and chemistry of azetidinones. Tetrahedron, 2003, 59: 7631–7649
4. Alcaide B, Almendros P, Aragoncillo C. β-Lactams: Versatile building blocks for the stereoselective synthesis of non-β-lactam products. Chem Rev, 2007, 107: 4437–4492
5. Cossío FP, Arrieta A, Sierra MA. The mechanism of the ketene-imine (Staudinger) reaction in its centennial: Still an unsolved problem. Acc Chem Res, 2008, 41: 925–936
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