Zum Verhalten von Olefinen,konjugierten Dienen und Steroidolefinen gegenüber Pb(OCOCF3)4 |
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Authors: | Dietmar Westphal Prof Dr Erich Zbiral |
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Institution: | (1) Organisch-Chemischen Institut der Universität Wien, Währinger Straße 38, A-1090 Wien, Österreich |
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Abstract: | The reaction of Pb(OCOCF3)4 with several olefines and conjugated dienes is reported. The oxidation of styrene, stilbene and 1.4-dihydro-1.4-methanonaphthalene leads to phenylacetaldehyde (1), benzaldehyde (2) and benzophenone (3), and to 1.2.3.4-tetrahydro-1.4-methanonaphthalene-(2S,9R+2R,9S)-diol-bis-trifluoroacetate (8) respectively. Of the conjugated dienes, 1.3-cyclohexadiene yieldscis-2-cyclohexene-1.4-diol bis-trifluoroacetate (4), cyclopentadiene yieldscis-2-cyclopentene-1.4-diolbis-trifluoroacetate (5) andtrans-2-cyclopentene-1.4-diol-bis-trifluoroacetate (6) andE,E-2.4-hexadiene yields the isomers of 3-hexene-2.5-diol bis trifluoroacetate (7). Oxidation of unsaturated steroids such as 2-cholestene, 2-androsten-17-one, 4-cholestene, androsta-4.9(11)-diene-3.17-dione and 3 -acetoxy-5-cholestene results in cholestane-2 ,3 -diol diacetate (9), 2 ,3 -diacetoxyandrostan-17-one (10) and 1 -acetoxy-2-androsten-17-one (11), in coprostane-4 ,5 -diol-4 -trifluoroacetate (12) or coprostane 4 ,5 -diol-4 -acetate (12a), 4-cholestanone (13), in 12 -trifluoroacetoxyandrosta-4,9(11)-diene-3.17-dione (14), and in cholestane-3 ,5 ,6 -triol-3 -acetate-6 -trifluoracetate.
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