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Gold(I)-Catalyzed Tandem Alkoxylation/Lactonization of γ-Hydroxy-α,β-Acetylenic Esters

✍ Scribed by Rubén S. Ramón; Christophe Pottier; Adrián Gómez-Suárez; Steven P. Nolan


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
248 KB
Volume
353
Category
Article
ISSN
1615-4150

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✦ Synopsis


The formation of 4-alkoxy-2(5H)-furan-A C H T U N G T R E N N U N G ones was achieved via tandem alkoxylation/lactonization of g-hydroxy-a,b-acetylenic esters catalyzed by 2 mol% of [2,6-bis(diisopropylphenyl)imidazol-2-ylidine]gold bis(trifluoromethanesulfonyl)imidate


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✍ Ge Gao; Qin Wang; Xiao-Qi Yu; Ru-Gang Xie; Lin Pu 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 1 views

g-Hydroxy-a,b-acetylenic esters containing three adjacent and structurally very different functional groups are very useful in the synthesis of highly functionalized organic molecules. [1, 2] This class of compound is normally prepared by treatment of an alkyl propiolate with nBuLi at À78 8C