ChemInform Abstract: A Novel Synthesis of 1,3-Diol Diesters by the Reaction of Aldehydes with Oxime Esters Catalyzed by Samarium Complex.
β Scribed by Y. KAWASAKI; D. TASHIRO; S. SAKAGUCHI; Y. ISHII
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
1998 carboxylic acid esters carboxylic acid esters (acyclic compounds) P 0360 21 -078 A Novel Synthesis of 1,3-Diol Diesters by the Reaction of Aldehydes with Oxime Esters Catalyzed by Samarium Complex.
-In connection with an earlier study the title reaction to esters such as (III) is developed. It is noteworthy that no reaction is observed in the presence of SmI 2 , SmI 3 and Sm(OTf) 3 . Other complexes such as Cp 2 Yb(thf) 2 are less effective. In the reaction with vinyl acetate (IV) the presence of (II) is important for the yield (17% yield in the absence of (II)). Mechanistical aspects are discussed.
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Enantioselective Aldol Reaction of Tin Enolates with Aldehydes Catalyzed by BINAPβ’Silver(I) Complex. -A new type of highly enantioselective aldol reactions of aldehydes with tributyltin enolates using the title complex as catalyst is described. Optimal conditions are established with THF as solvent