95891-76-2Relevant articles and documents
Diethylaluminum ethoxide mediated crossed aldol reaction of enol esters with carbonyl compounds
Mukaiyama, Teruaki,Shibata, Jun,Shimamura, Tadashi,Shiina, Isamu
, p. 951 - 952 (1999)
Crossed aldol reaction of enol esters, stable carbon nucleophiles, with carbonyl compounds is effectively performed by the promotion of diethylaluminum ethoxide under mild conditions. This reaction is applicable not only to simple enol esters but also to
Aldol-Type Reaction by Propen-2-yl Acetate with NCS/SnCl2/ROH
Masuyama, Yoshiro,Kobayashi, Yumiko,Yanagi, Ryota,Kurusu, Yasuhiko
, p. 2039 - 2042 (2007/10/02)
The addition of N-chlorosuccinimide (NCS) to a solution of propen-2-yl acetate, aldehydes, SnCl2, and benzyl alcohol in CH2Cl2 or CH3CN caused an aldol-type reaction to produce 4-substituted 4-benzyloxybutan-2-ones in high yields.Use of methanol instead of benzyl alcohol produced not only 4-methoxybutan-2-one but also 3-buten-2-one by dehydromethoxylation.
Facile Synthesis of Acyl-Substituted Lactone Derivatives from Acyclic Keto Esters
Miller, Robert D.,Fickes, Garry N.
, p. 2375 - 2377 (2007/10/02)
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