Michael-type addition of O-ethyl-C,O-bis(trimethylsilyl)ketene acetal and its application to the synthesis of α-ylidene-δ-lactones
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference20 articles.
1. Stereocontrolled synthesis of α,β-unsaturated carboxylic esters from O-methyl-C,O-bis(trimethylsilyl)ketene acetal and aliphatic aldehydes
2. Convenient synthesis of jasmonoid compounds from .gamma.-(trimethylsiloxy)butyronitrile
3. Carbonyl olefination reaction using silyl-substituted organometallic compounds
4. A New Synthesis of α,β-Unsaturated Carboxylic Esters. The Condensation of Ethyl Lithiotrimethylsilylacetate with Carbonyl Compounds
5. Reaction of lithio -butyl trimethylsilylacetate with aldehydes and ketones. A synthesis of α,β-unsaturated esters.
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2. Formation of Aldehydes and Ketones by 1,4‐Addition to α,β‐Unsaturated Carbonyl Compounds and Derivatives;Comprehensive Organic Transformations;2018-02-28
3. N-heterocyclic carbene-catalysed Peterson olefination reaction;Tetrahedron;2016-01
4. A Convenient Method for the Lewis Base-catalyzed Synthesis of α,β-Unsaturated Carboxylic Esters Using Trimethylsilylketene Ethyl Trimethylsilyl Acetal and Carbonyl Compounds;Chemistry Letters;2008-07-05
5. Titanocene(III) Chloride Mediated Radical-Induced Addition to Baylis−Hillman Adducts: Synthesis of (E)- and (Z)-Trisubstituted Alkenes and α-Methylene/Arylidene δ-Lactones;The Journal of Organic Chemistry;2008-04-22
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