1955
DOI: 10.1111/j.2042-7158.1955.tb12006.x
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Ascaridole Studies: Part III. The Purification and Characterisation of Ascaridole

Abstract: 1 3 4 5 6 7 8 9 10 11 12 This Paper b.pt., O c. 84/3 mm. 96 to 97/8 mm. 80 to 81/4 mm. 85 to 95/2-5 mm. 113 to 1l4/20 mm. l l 5 j l S mm. -75/13 mm. 83 to 84/3 mm. 83/4-5 mm. 115/15 mm., 8415 mm. 3940/0.2 mm. m.pt., c. -n200 C.' * 0.00" Assay (per cent. v/w ascaridole, iodimetric method) 110.8Authors' values of n, !, -recalculated by applying a correction of -04004 per degree rise of temperature (see later) to enable comparison at 20' C. to be made.

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Cited by 11 publications
(2 citation statements)
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“…The first isolation of the most active component-ascaridole ( 174 ), from the Chenopodium ambrosioides and the determination of its structure was dated to the beginning of the last century [ 109 , 110 , 111 , 112 ]. In the 1950s, the ascaridole ( 174 ) was completely characterized ( Scheme 26 ) [ 113 , 114 ].…”
Section: 12-dioxenesmentioning
confidence: 99%
“…The first isolation of the most active component-ascaridole ( 174 ), from the Chenopodium ambrosioides and the determination of its structure was dated to the beginning of the last century [ 109 , 110 , 111 , 112 ]. In the 1950s, the ascaridole ( 174 ) was completely characterized ( Scheme 26 ) [ 113 , 114 ].…”
Section: 12-dioxenesmentioning
confidence: 99%
“…The simple endoperoxide of bisabolene (92) (1 13) (111) LOB"' 0 related nor-sesquiterpene, senedigitalen-1,4-endoperoxide (93), was isolated from another Senecio species, S. paludaflnis. 123 An inseparable mixture of two bisabolol hydroperoxides, (94) and ( 95), was isolated from Schistostephium crataegif o 1 i ~m .…”
Section: Bisabolene Derivativesmentioning
confidence: 99%