1993
DOI: 10.1016/s0040-4039(00)73546-5
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Synthesis of pinacol silylethers from aromatic aldehydes via α-siloxybenzyliron complexes

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Cited by 8 publications
(2 citation statements)
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“…By using a larger excess of p -anisaldehyde, the yield of 7c was improved from 52% to 62%. A major byproduct in the synthesis of 7c was the dimer [In(CO) 2 Fe] 2 . , Minor byproducts included the silyl complex In(CO) 2 Fe−SiMe 3 and the pinacol silyl ether [( p -OCH 3 Ph)CH−(OSiMe 3 )] 2 ,9b the latter is thought to be formed by decomposition of the product 7c …”
Section: Resultsmentioning
confidence: 99%
“…By using a larger excess of p -anisaldehyde, the yield of 7c was improved from 52% to 62%. A major byproduct in the synthesis of 7c was the dimer [In(CO) 2 Fe] 2 . , Minor byproducts included the silyl complex In(CO) 2 Fe−SiMe 3 and the pinacol silyl ether [( p -OCH 3 Ph)CH−(OSiMe 3 )] 2 ,9b the latter is thought to be formed by decomposition of the product 7c …”
Section: Resultsmentioning
confidence: 99%
“…85 Pinacol silyl ethers 141 can also be prepared from the complexes 138 by thermodecomposition at 60 °C in 48-88% yield (Scheme 42). 87 The only byproduct formed in these reactions is the dimer 1 (see,…”
Section: Scheme 41mentioning
confidence: 99%