Stereoselective conjugate addition - alkylations of α,β-unsaturated iron acyls
✍ Scribed by Lanny S. Liebeskind; Mark E. Welker
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 199 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Conjugate additions and conjugate ad$ition-alkylations proceed with very high stereoselectivity to a,&unsaturated acyls of n -CpFe(CO)(PPh ). 2
Oxidative cleavage of the products provides high yields of organic acid derivatives (es ers, B-lactams) with almost complete control of relative stereochemistry.
📜 SIMILAR VOLUMES
We recently reported the first examples of conjugate additions of alkyl sulphoxides to unsaturated esters,\* These reactions proceed with good selectivity and provide a promising new method for carrying out
A new asymmetric synthesis of both enantiomers of P-substituted ketones is described. Our recent investigation on the chemistry of activating a chiral protecting group by organometallic reagents' has prompted us to report a stereoselective conjugate addition of organoaluminum compounds to chiral o,
Summaqv: The reaction of Iithiated a&l t-butyl sulphoxides with a&unsaturated esters gives conjugate addition products in good yield, with high stereoselectivity. Asymmetric conjugate additions to a&unsaturated carbonyl compounds have been the subject of (
## UtiaAw&ed acy&tian~n hehue M kigkey heactive cahboxytic acid eqtiva_&nts in conjugate &yLation ma&ions with &ykkXane de,tivtivw.