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- W2330258932 abstract "Umsetzung des chiralen Diols (Ib), erhältlich aus dem Hydroxyketon (Ia) mit Phenyl-Li; mit den Allylboranen (II) liefert die optisch aktiven Boronsäureester (III), die mit den Aldehyden (IV) zu den Borsäureestern (V) reagieren; nachfolgende Spaltung mit Nitrilotriethanol gibt die chiralen Alkohole (VI), die jeweils mit überwiegendem Anteil eines Enantiomeren ((R)- oder (S)-) anfallen (Enantiomerenüberschuß: 45 bis 77%)." @default.
- W2330258932 created "2016-06-24" @default.
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- W2330258932 date "1979-01-16" @default.
- W2330258932 modified "2023-10-18" @default.
- W2330258932 title "ChemInform Abstract: ENANTIOSELECTIVE SYNTHESIS OF HOMOALLYL ALCOHOLS VIA CHIRAL ALLYL BORIC ACID ESTERS" @default.
- W2330258932 cites W2125229110 @default.
- W2330258932 doi "https://doi.org/10.1002/chin.197903080" @default.
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