Base-dependent stereoselectivity in reactions of acyl ligand in phenylacetyliron complex (η5-C5H5)Fe(CO)(PPh3)(COCH2Ph)
✍ Scribed by Zhong-Wu Guo; Aleksander Zamojski
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 253 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Alkylation of the anion 4 is only little stereoselective und leads to mixtures of stereoisumeric products SA&9A,B. Proportion qf stereoisomers depends strongly on the base employed. Condensation with acetaldehyde or benzaldehyde leads to four stereoisomeric products llC-F and 12C-F, proportion of which depends also on the bases used.Decomplexation leadr in fhe case of alkylutedproducts to bromides 13, and in the cuse of uldolproduct 11 to brontohydrin 14 and epoxides 1.5 and Id.
📜 SIMILAR VOLUMES
## Application of the Iron Acyl Complex (S)-(+)-[(115-CsHs)Fe(CO)(PPh3)COCHzPh] as a Homochiral Phenylacetate Enolate Equivalent,
## Surnmnry: The enantiomerically pure iron acyl complex R-(-)-[($-CSH5)Fe(CO)(PPh3)-CUCH20({lR,2S,5R]menthyl))] tepresents a source of homochiral formyl anion equivalent applicable to the synthesis of enantiomerkally pare a-hydroxy acetals from aldehydes. The formyl anion or a synthetic equivale