1956
DOI: 10.1021/ja01588a042
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Santonin. II.1 The Synthesis of New Stereoisomers of Santonin2

Abstract: Yol. 78 solid was filtered, washed with water and dried to give 37.9 g., m.p. 200-211°. After digestion for one hour with 350 ml. of boiling acetone, there was obtained 24.9 g. (66%) of X, m.p. 217-222°.The analytical sample was recrystallized from ethanol and had m.p. 225.5-228.5°, [a]o +110°(1% in dioxane).

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Cited by 11 publications
(2 citation statements)
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“…The C-C bond formation process takes place in d-position. A 1,7-difunctional compound is the result of this reaction [50].…”
Section: 7-difunctional Compoundsmentioning
confidence: 99%
“…The C-C bond formation process takes place in d-position. A 1,7-difunctional compound is the result of this reaction [50].…”
Section: 7-difunctional Compoundsmentioning
confidence: 99%
“…The two products, as they turned out, were the ketones (12) and (13) with no trace of the expected ene alcohol (10). The saturated ketone (12) showed in its i.r. spectrum a ketone carbonyl band at 1 710 cm-' whereas the unsaturated ketone (13) showed the same band at 1 670 cm-' besides other bands.…”
mentioning
confidence: 99%