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Kwart, H.; Khan, A. A. J. Am. Chem. Soc. 1967, 89 , 1951–1953. Breslow, R.; Gellman, S. H. J. Chem. Soc., Chem. C PowerPoint Presentation
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Kwart, H.; Khan, A. A. J. Am. Chem. Soc. 1967, 89 , 1951–1953. Breslow, R.; Gellman, S. H. J. Chem. Soc., Chem. C

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Kwart, H.; Khan, A. A. J. Am. Chem. Soc. 1967, 89 , 1951–1953. Breslow, R.; Gellman, S. H. J. Chem. Soc., Chem. C - PowerPoint PPT Presentation


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Kwart, H.; Khan, A. A. J. Am. Chem. Soc. 1967, 89 , 1951–1953. Breslow, R.; Gellman, S. H. J. Chem. Soc., Chem. Comm. 1982, 1400–1401. Breslow, R.; Gellman, S. H. J. Am. Chem. Soc. 1983 , 105, 6728–6729. Müller, P. et al. Tetrahedron 1996 , 52 , 1543–1548.

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slide5

Kwart, H.; Khan, A. A. J. Am. Chem. Soc. 1967,89, 1951–1953.

Breslow, R.; Gellman, S. H. J. Chem. Soc., Chem. Comm. 1982, 1400–1401.

slide7

Müller, P. et al. Tetrahedron 1996, 52, 1543–1548.

Müller, P. et al. Helv. Chim. Acta 1997, 80, 1087–1105.

slide28

General reactivity trend: 3° > α-ethereal ≥ benzylic > 2° >> 1°

Du Bois, J. et al. J. Am. Chem. Soc. 2007, 129, 562-568.

slide42
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