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pro vyhledávání: '"D. H. Thorpe"'
The late 1970s saw the emergence of a heated debate on the treatment of juvenile delinquents. The argument was usually presented as being between the exponents of ‘law and order'and punishment on the one hand, and the ‘soft'advocates of social wo
Publikováno v:
Journal of Endocrinology. 78:389-397
The breeding seasons of two groups of pinealectomized ferrets and one group of blind ferrets, with appropriate controls, were observed for up to 5 years after the operations. All animals showed recurrent breeding seasons. Both pinealectomized and bli
Autor:
D H, Thorpe
Publikováno v:
Anesthesia and analgesia. 63(2)
Autor:
D H, Thorpe
Publikováno v:
The Journal of endocrinology. 49(3)
Publikováno v:
Chemischer Informationsdienst. 4
Publikováno v:
Chemischer Informationsdienst. 4
Autor:
P. Mazel, A. C. Robichaux, John B. Craft, H. S. Kim, D. H. Thorpe, W. A. Woolf, A. L. Stolte, Julius Neumark
Publikováno v:
Obstetric Anesthesia Digest. 4:148
Autor:
D. H. Thorpe, J. M. Birchall
Publikováno v:
Journal of the Chemical Society C: Organic. :2071
The Fries-type rearrangement of N-benzoyldiphenylamine in the presence of polyphosphoric acid at 130° affords 4,4′-dibenzoyldiphenylamine, 9-phenylacridine, and 2,7-dibenzoyl-9-phenylacridine. The same products, together with N-benzoyldiphenylamin
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :442
N-Benzoyl-, N-(p-toluoyl)-, and N-(p-chlorobenzoyl)-diphenylamine react with an excess of aluminium chloride at 140–180° to give the corresponding 4,4′-diaroyldiphenylamines and diphenylamine itself. N,4-Dibenzoyldiphenylamine gives only 4,4′-
Autor:
D. H. Thorpe, J. M. Birchall
Publikováno v:
Journal of the Chemical Society C: Organic. :2900
The rearrangement of N-anisoyl-, N-(p-chlorobenzoyl)- or N-(p-nitrobenzoyl)-diphenylamine in polyphosphoric acid at 110–160° yields mainly the corresponding 9-arylacridine with, in the first two cases, diphenylamine and the 4,4′-diaroyldiphenyla