Literature DB >> 24573792

Organocatalytic enantioselective decarboxylative aldol reaction of malonic acid half thioesters with aldehydes.

Han Yong Bae1, Jae Hun Sim, Ji-Woong Lee, Benjamin List, Choong Eui Song.   

Abstract

Entities:  

Keywords:  aldehydes; aldol reaction; organocatalysis; reaction mechanisms; synthetic methods

Year:  2013        PMID： 24573792     DOI： 10.1002/anie.201306297

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  7 in total

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2.  Pictet-Spengler reaction-based biosynthetic machinery in fungi.

Authors:  Wei Yan; Hui Ming Ge; Gang Wang; Nan Jiang; Ya Ning Mei; Rong Jiang; Sui Jun Li; Chao Jun Chen; Rui Hua Jiao; Qiang Xu; Seik Weng Ng; Ren Xiang Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-25       Impact factor: 11.205

Review 3.  Chemical Batteries with CO2.

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4.  Regioselective decarboxylative addition of malonic acid and its mono(thio)esters to 4-trifluoromethylpyrimidin-2(1H)-ones.

Authors:  Sergii V Melnykov; Andrii S Pataman; Yurii V Dmytriv; Svitlana V Shishkina; Mykhailo V Vovk; Volodymyr A Sukach
Journal:  Beilstein J Org Chem       Date:  2017-12-07       Impact factor: 2.883

5.  Biomimetic catalytic transformation of toxic α-oxoaldehydes to high-value chiral α-hydroxythioesters using artificial glyoxalase I.

Authors:  Sang Yeon Park; In-Soo Hwang; Hyun-Ju Lee; Choong Eui Song
Journal:  Nat Commun       Date:  2017-04-04       Impact factor: 14.919

6.  Selective acceleration of disfavored enolate addition reactions by anion-π interactions.

Authors:  Yingjie Zhao; Sebastian Benz; Naomi Sakai; Stefan Matile
Journal:  Chem Sci       Date:  2015-08-25       Impact factor: 9.825

7.  The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst.

Authors:  Deniz Tözendemir; Cihangir Tanyeli
Journal:  Beilstein J Org Chem       Date:  2021-02-18       Impact factor: 2.883
  7 in total

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