The reductive alkylation of aniline
WS Emerson, PM Walters
Index: Emerson; Walters Journal of the American Chemical Society, 1938 , vol. 60, p. 2024
Full Text: HTML
Citation Number: 7
Abstract
Summary A convenient method for the catalytic dehydrogenation of sugar alcohols was developed. Mannitol and dulcitol were the hexitols studied. The advantage of the method lies in the ease of controlling the amount of hexitol dehydrogenated. The results obtained indicate that the method is most satisfactory for aldose isolation in the case of alcohols which yield but one aldose or a dl-aldose when dehydrogenated. Platinic oxide monohydrate ...
Related Articles:
[Del Pozo, Carolina; Corma, Avelino; Iglesias, Marta; Sanchez, Felix Journal of Catalysis, 2012 , vol. 291, p. 110 - 116]
A novel strategy for N-alkylation of primary amines
[Srivastava, Sanjay K.; Chauhan, Prem Man Singh; Bhaduri, Amiya P. Synthetic Communications, 1999 , vol. 29, # 12 p. 2085 - 2091]
[Del Pozo, Carolina; Corma, Avelino; Iglesias, Marta; Sanchez, Felix Journal of Catalysis, 2012 , vol. 291, p. 110 - 116]
[Bhor, Malhari D.; Bhanushali, Mayur J.; Nandurkar, Nitin S.; Bhanage, Bhalchandra M. Tetrahedron Letters, 2008 , vol. 49, # 6 p. 965 - 969]
The reductive alkylation of aniline
[Emerson; Walters Journal of the American Chemical Society, 1938 , vol. 60, p. 2023]