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A study of the aldol reaction between enolates derived from the iron acetyl complex [(η5-C5H5)Fe(CO)(PPh3)COCh3] and 2,3-O-lsopropylidene-D-glyceraldehyde

✍ Scribed by Graham J. Bodwell; Stephen G. Davies; Andrew A.6Mortlock

Book ID
108374290
Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
773 KB
Volume
47
Category
Article
ISSN
0040-4020

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📜 SIMILAR VOLUMES

Application of the iron acyl complex R-(
Application of the iron acyl complex R-(-)-[(η5-C5H5)Fe(CO)(PPh3)- COCH2O({{1R,2S}},5Rmenthyl)] as a homochiral formyl anion equivalent
✍ Stephen G. Davies; David Middlemiss; Alan Naylor; Martin Wills 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 307 KB

## 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

Asymmetric synthesis of (S)-(−)-methyl t
Asymmetric synthesis of (S)-(−)-methyl tropinate: application of the iron acyl complex (S)-(+)-[(η5-C5H5)Fe(CO)(PPh3)COCH2Ph] as a homochiral phenylacetate enolate equivalent.
✍ Teresa M Baker; Graham J Bodwell; Stephen G Davies; Alison J Edwards; Michael R 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 892 KB

## Application of the Iron Acyl Complex (S)-(+)-[(115-CsHs)Fe(CO)(PPh3)COCHzPh] as a Homochiral Phenylacetate Enolate Equivalent,