Lewis and mediated α-alkylation of ketones using SN1 reactive alkylating agents
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (51), 4971-4974
- https://doi.org/10.1016/s0040-4039(01)86764-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- α-Alkylation of ketones, esters, and lactones: zinc bromide-catalysed alkylation of o-silylated enolates, a synthesis of (±)-ar-turmeroneTetrahedron Letters, 1979
- Regiospecific α-methylenation and α-methylation of ketones: titanium tetrachloride promoted phenylthiomethylation of silyl enol ethersTetrahedron Letters, 1979
- α-Alkylation and α-alkylidenation of carbonyl compounds: Lewis acid-promoted phenylthioalkylation of o-silylated enolatesTetrahedron Letters, 1979
- α-tert-alkylierung von carbonsäure-esternTetrahedron Letters, 1978
- tert‐Alkylierung von Ketonen und AldehydenAngewandte Chemie, 1978
- α-t-Butylation of aldehydes and ketones by the Friedel-Crafts alkylation of trimethylsilyl enol ethersTetrahedron Letters, 1977
- Titantetrachlorid in der organischen SyntheseAngewandte Chemie, 1977
- Chemistry of enolates. VI. Acidity scale for ketones. Effect of enolate basicity in elimination reactions of halidesThe Journal of Organic Chemistry, 1968