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- W2014577931 abstract "6-endo-Chlorcampheroxim (1) reagiert mit 65proz. Schwefelsäure zu 3-Chlor-β-campholenonitril (3), cis-3-Chlor-dihydro-β-campholenolacton (4), trans-3-Chlor-dihydro-β-campholenolacton (5) und einem höheren Kohlenwasserstoff. Beckmann Rearrangement of 6-endo-Chlorocamphor Oxime 6-endo-Chlorocamphor oxime (1) reacts with sulfuric acid (65%) to give 3-chloro-β-campholenonitrile (3), cis-3-chlorodihydro-β-campholenolactone (4), trans-3-chlorodihydro-β-campholenolactone (5) and a higher alkane." @default.
- W2014577931 created "2016-06-24" @default.
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- W2014577931 date "1977-01-01" @default.
- W2014577931 modified "2023-10-09" @default.
- W2014577931 title "Zur Beckmann-Umlagerung von 6- e n d o -Chlorcampheroxim" @default.
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- W2014577931 doi "https://doi.org/10.1002/ardp.19773100114" @default.
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