Synthetic methods. 19. Lewis acid catalyzed conversion of alkenes and alcohols to azides

A Hassner, R Fibiger, D Andisik

Index: Hassner, Alfred; Fibiger, Richard; Andisik, Donald Journal of Organic Chemistry, 1984 , vol. 49, # 22 p. 4237 - 4244

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Citation Number: 58

Abstract

(m, 2, CH2CH2CH3), 2.22-2.32 (m, 2), 2.51 (t, J = 8 Hz, 2, CH2CH2CH3), 2.73 (t, J = 8 Hz, 2, benzylic H), 5.96-6.08 (m, 1, C-2 vinylic H), 6.42 (d, J = 10 Hz, 1, C-1 vinylic H), 6.84-7.04 (m, 3, aromatic H); I3C NMR (CDCl,) 6 27.1 (Cl), 23.3 (C-2), 127.9 ((2-3 or 4), 128.4 (C-3 or 4), 126.1 (C-5), 140.7 (C-6), 126.8 ((2-7 or 8), 127.3 (C-7 or 8), 132.6 (C-9), 133.9 (C-lo), 13.8 (CH&H2CH3), 24.6 (CH2CH2CH3), 37.7 (CH2CH2CH3); mass spectrum (70 eV), m/ ...

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