1995
DOI: 10.1016/0040-4020(94)01020-z
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Conjugate addition reactions of metallated alkyl pyridines. A direct route to 6-substituted pyridones

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Cited by 6 publications
(1 citation statement)
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“…Simultaneous desulfurisation and debenzylation using RaNi leads to the pyridone 298. 463 The keto silane 299 is reduced by Li-NH, to give the hydroxy silane 300 which reacts with Bu4NF followed by H202 to give the diol 301 with retention of stereochemistry at the C-Si centre. 464 The latter steps of the sequence provide a method for the conversion of a silane into an alcohol in the presence of an olefinic bond.…”
Section: Pest-control Agents Have Attracted Attention (R)-( +)-mentioning
confidence: 99%
“…Simultaneous desulfurisation and debenzylation using RaNi leads to the pyridone 298. 463 The keto silane 299 is reduced by Li-NH, to give the hydroxy silane 300 which reacts with Bu4NF followed by H202 to give the diol 301 with retention of stereochemistry at the C-Si centre. 464 The latter steps of the sequence provide a method for the conversion of a silane into an alcohol in the presence of an olefinic bond.…”
Section: Pest-control Agents Have Attracted Attention (R)-( +)-mentioning
confidence: 99%