Chelation-controlled reduction of α- and β-oxygenated ketones with lithium tri-n-butylborohydride
✍ Scribed by Anne-Marie Faucher; Christian Brochu; Serge R. Landry; Isabelle Duchesne; Susanne Hantos; Amélie Roy; Andrew Myles; Claude Legault
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 291 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Press Ltd. printed in Great Britain, SPECIFIC DEXITFXUTION PTOAl&TO mOUP t RFXIUCTION OF a k -cKCTONEY WITliLITHIOMANDDEDTEZA~DPROPYIAH~ Marcel FH'IZON andJacques GORE LaboratoFre de St&dochimie -Facult6 des Soienoea d'Orsay -(S et O)BRAN(X (Received 3 December 1965) Whereas the introduction of a de
The reduction of ct-alkyl-13-hydroxy ketones is highly syn-seleetive if carried out in THF on their Ti-alcoholate complexes with LiBI-h or L-SeleetrideCg or N-sclectride~ depending on the bulkiness of the group bound to the earbonyl group.