99865-03-9Relevant articles and documents
A Single-Flask Synthesis of Morita-Baylis-Hillman Adducts from Ethoxyacetylene and Carbonyl Compounds: Synthesis of Subamolides D and e
Ng, Kevin,Minehan, Thomas G.
, p. 4028 - 4031 (2016)
Sequential treatment of (ethoxyethynyl)lithium with aldehydes and/or ketones (2 and 4) and BF3·OEt2 gives rise to β-hydroxyenoates 5 in good to excellent overall yields. Similarly, the combination of 1 (M = Li) and dicarbonyl compounds 6 (X = O) or keto/aldehyde acetals (X = OMe) followed by the addition of a Lewis acid leads to five-, six-, and seven-membered hydroxycycloalkene carboxyates. The utility of this method is demonstrated in the synthesis of the α-alkylidene lactone natural products subamolide D and E.
A Convenient Procedure for the Preparation of Ethoxyacetylene and Ethoxyethynyl Carbinols
Raucher, Stanley,Bray, Brian L.
, p. 2332 - 2333 (2007/10/02)
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