1997
DOI: 10.1002/(sici)1099-1344(199703)39:3<215::aid-jlcr961>3.0.co;2-e
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Synthesis of 3H labeled dihydrorotenone
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Cited by 8 publications
(4 citation statements)
References 13 publications
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Abstract
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“…However, the multi‐step synthesis of 4 proceeds via intermediate 5 (shown in Scheme ), which was present in abundance and ready to use. Furthermore, it has been reported in the literature that under standard reaction conditions for tritio‐dehalogenations, using Pd/C and tritium gas, C═C double bonds may undergo saturation or isomerisation, even at low tritium pressures . Intermediate 5 , unlike 4 , does not contain a double bond and, therefore, did not appear at risk to undergo an unwanted reduction.…”
Section: Results
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…However, the multi‐step synthesis of 4 proceeds via intermediate 5 (shown in Scheme ), which was present in abundance and ready to use. Furthermore, it has been reported in the literature that under standard reaction conditions for tritio‐dehalogenations, using Pd/C and tritium gas, C═C double bonds may undergo saturation or isomerisation, even at low tritium pressures . Intermediate 5 , unlike 4 , does not contain a double bond and, therefore, did not appear at risk to undergo an unwanted reduction.…”
Section: Results
mentioning
confidence: 99%
Abstract
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“…Because no details were reported for the preparation of 25 , Williams and colleagues at the former Berkeley National Tritium Labelling Facility studied its tritium labeling in greater depth . These radiochemists employed the tritiation conditions displayed in Scheme and in the course of their radiolabeling reported another single contaminant accompanying desired product 25 .…”
Section: [3h]dihydrorotenone
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confidence: 99%
Abstract
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“…These signals are attributed to tritium incorpoation at the 6¢ (exocyclic methine), 7¢, and 8¢ (methyl) positions. 86…”
Section: Reduction Of Carbon-carbon Double and Triple Bonds
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confidence: 99%
