Literature DB >> 25246085

Decarboxylative allylations of ester enolate equivalents.

Yamuna Ariyarathna1, Jon A Tunge.   

Abstract

A variety of ester enolate equivalents are generated in situ and undergo α-allylation in high yields via palladium-catalyzed decarboxylative allylation. The transformations are complete within very short reaction times under ambient conditions. Synthesis of α-allylated acyl derivatives provides access to other carboxylic acid and alcohol derivatives via acyl group substitution or reduction.

Entities:  

Year:  2014        PMID: 25246085     DOI: 10.1039/c4ob01752h

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Catalytic Enantioselective Synthesis of α-Difunctionalized Cyclic Sulfones.

Authors:  Eleanor Bowen; Gillian Laidlaw; Bethany C Atkinson; Timur A McArdle-Ismaguilov; Vilius Franckevičius
Journal:  J Org Chem       Date:  2022-07-08       Impact factor: 4.198

2.  Ruthenium-catalyzed decarboxylative C-S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide.

Authors:  Ren-Hua Zheng; Hai-Chang Guo; Ting-Ting Chen; Qing Huang; Guo-Bo Huang; Hua-Jiang Jiang
Journal:  RSC Adv       Date:  2018-07-12       Impact factor: 3.361

3.  On the hydrolysis of diethyl 2-(perfluorophenyl)malonate.

Authors:  Ilya V Taydakov; Mikhail A Kiskin
Journal:  Beilstein J Org Chem       Date:  2020-07-28       Impact factor: 2.883

  3 in total

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