The synthesis of secondary and tertiary amines by borohydride reduction1
KA Schellenberg
Index: Schellenberg,K.A. Journal of Organic Chemistry, 1963 , vol. 28, p. 3259 - 3261
Full Text: HTML
Citation Number: 108
Abstract
Yieldb of. 4cetone,'M NaBHI. M total PH Ne-isopropyllysine,% 2.4' 0.4 d 4.1-4.7 4 2.4= 0.9 d 4.1-4.7 15 2.4" 1.8 d 4.1-4.7 34 2.4 c 3.6 d 4.1-4.7 46 2.4" 7. Zd 4.1-4.7 50 0.6 c 2. Id 4.1-4.7 8 1.1" 2.0 d 4.1-4.7 26 4.1 C 1.5 d 4.1-4.7 53 2.4 e 1. Sd 6.1 (initial) 6 2.4' 1.8' 6.3-6.7 55 2.40 1.89 11 20
Related Articles:
[Henze; Humphreys Journal of the American Chemical Society, 1942 , vol. 64, p. 2879,2880]
[Howk et al. Journal of the American Chemical Society, 1954 , vol. 76, p. 1899,1901]
[Burton, Allen W. Journal of the American Chemical Society, 2007 , vol. 129, # 24 p. 7627 - 7637]
[D'Arcy,R. et al. Helvetica Chimica Acta, 1966 , vol. 49, p. 185 - 203]