ChemInform Abstract: Reformatsky-Type Addition of Esters of α-Halogeno Carboxylic Acids to Aldehydes and Ketones in the Presence of Fe(CO)5.
✍ Scribed by A. B. Terent'ev; T. T. Vasil'eva; N. A. Kuz'mina; E. I. Mysov; N. S. Ikonnikov; N. Yu. Kuznetsov; Yu. N. Belokon
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 37 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Reformatsky-Type Addition of Esters of α-Halogeno Carboxylic Acids to Aldehydes and Ketones in the Presence of Fe(CO) 5 .
-Fe(CO) 5 -promoted Reformatsky-type addition of α-halogenocarboxylates to carbonyl compounds affords the corresponding β-hydroxycarboxylates (III) (12 examples) in moderate to good yields. α-Polyhalogenated carboxylates (IV) react substantially different under similar conditions and provide esters of substituted acrylic acids (VI)/(VII). -(TERENT'EV, A.
📜 SIMILAR VOLUMES
Addition of Thiols to α,β-Unsaturated Esters in the Presence of Alumina. -Michael-type additions of thiols to α,β-unsaturated esters in the presence of neutral alumina proceed easily under appropriate mild conditions to give the corresponding adducts [cf. (III), (VI)/(VII)] in good to excellent yie
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Asymmetric 1,4 Addition of Grignard Reagents to Chiral α,β-Unsaturated Esters in the Presence of Lewis Acids. -The reaction proceeds with good yields but variable diastereoselectivities, depending on the organometallic reagent and Lewis acid used. -(CARDILLO, GIULIANA;