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A novel ketone synthesis by a palladium-catalyzed reaction of thiol esters and organozinc reagents

โœ Scribed by Hidetoshi Tokuyama; Satoshi Yokoshima; Tohru Yamashita; Tohru Fukuyama


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
241 KB
Volume
39
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


A variety of ketones have been prepared by a palladium-catalyzed reaction of ethanethiol esters with organozinc reagents. Various functional groups, including esters, ketones, aromatic halides and aldehydes, tolerate the reaction conditions. The reaction can also be applied to the synthesis of t~-amino ketones using the corresponding L-Or-amino thiol esters without racemization.


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Stereocontrolled synthesis of (+)-lycope
โœ Hidekazu Masaki; Tomoko Mizozoe; Tomoyuki Esumi; Yoshiharu Iwabuchi; Susumi Hata ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 147 KB

An ecient stereocontrolled synthesis of (+)-lycoperdic acid has been achieved based on palladium catalyzed cross-coupling reaction of (Z)-1-(tert-butyldimethylsiloxy)-3-iodo-6-(p-methoxybenzyl)oxy-2-hexene with the organozinc reagent, prepared from N-Boc-b-iodoalanine methyl ester.