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Skatole as a Root Forming Substance
Nature, 1937THE activity of skatole as a growth-promoting substance has been noted by Glover1. We have carried out experiments which show that skatole accelerates root formation in cuttings. Cuttings of Leptospermum sooparium and of Ficus repens were treated with an aqueous solution of skatole in the manner described by Hitchcock and Zimmerman2, and the cuttings ...
L. G. G. WARNE, A. A. JACKSON
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Mechanism and Stereoselectivity of the BINOL-Catalyzed Allylboration of Skatoles
Organic Letters, 2017Density functional theory calculations have been performed to investigate the binaphthol-catalyzed allylboration of skatoles. The high stereoselectivity observed for the reaction is reproduced well by the calculations and was found to be mainly a result of steric repulsions in the corresponding Zimmerman-Traxler transition states.
Genping Huang +3 more
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Preliminary observations on skatole production in pigs
Proceedings of the British Society of Animal Production (1972), 1989Skatole and indole, compounds formed in the large intestine by microbial breakdown of tryptophan, are associated with carcass taint (Hansson et al., 1980). The present work involved the development of a method for detecting the absolute values of the analytes in fat and faeces.
M. Hawe, N. Walker, M. Porter, B.W. Moss
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Skatole as a Growth-Promoting Substance
Nature, 1936INDOLE has been described as being inactive by Thimann and Koepfli1, but skatole ( methyl indole) was apparently not tested. Pure skatole was obtained from B.D.H. and was twice recrystallised to remove possible impurities. Bending experiments were performed using oat coleoptiles (Argentine VI).
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Electrophilic substitution in skatole and its derivatives
Tetrahedron, 1958Abstract Evidence is presented to show that the 2-position is the primary site of electrophilic substitution in skatole and its derivatives. Existing data in the literature are reconciled with this view.
Wayland E. Noland, Donald N. Robinson
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6-Hydroxyskatole Glucuronide, a Skatole Metabolite
Nature, 1966THE metabolism of 6-hydroxylated indoles is of interest in view of their possible psychotoxicity as reported by Szara1 and the finding, originally by Leyton2, that 6-hydroxyskatole sulphate is excreted in larger amounts by schizophrenic patients.
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An unusual reaction of skatole with tetranitromethane
Journal of the American Chemical Society, 1969T F, Spande, A, Fontana, B, Witkop
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Occurrence, impacts, and microbial transformation of 3-methylindole (skatole): A critical review
Journal of Hazardous Materials, 2021Qiao Ma
exaly