Literature DB >> 19746510

Organocatalytic enantioselective cross-aldol reactions of aldehydes with isatins: formation of two contiguous quaternary centered 3-substituted 3-hydroxyindol-2-ones.

Fei Xue1, Shilei Zhang, Lu Liu, Wenhu Duan, Wei Wang.   

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Year:  2009        PMID： 19746510     DOI： 10.1002/asia.200900243

Source DB:  PubMed          Journal:  Chem Asian J        ISSN： 1861-471X


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  5 in total

1.  Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.

Authors:  Qunsheng Guo; Mayur Bhanushali; Cong-Gui Zhao
Journal:  Angew Chem Int Ed Engl       Date:  2010-12-03       Impact factor: 15.336

2.  Asymmetric Aldol Reaction of 3-Acetyl-2H-chromen-2-ones and Isatins Catalyzed by a Bifunctional Quinidine Urea Catalyst.

Authors:  Santhi Abbaraju; John Cong-Gui Zhao
Journal:  Adv Synth Catal       Date:  2014-01-13       Impact factor: 5.837

3.  Bioconversion of Biologically Active Indole Derivatives with Indole-3-Acetic Acid-Degrading Enzymes from Caballeronia glathei DSM50014.

Authors:  Mikas Sadauskas; Roberta Statkevičiūtė; Justas Vaitekūnas; Rolandas Meškys
Journal:  Biomolecules       Date:  2020-04-24

4.  Enantioselective solvent-free synthesis of 3-alkyl-3-hydroxy-2-oxoindoles catalyzed by binam-prolinamides.

Authors:  Abraham Bañn-Caballero; Jesús Flores-Ferrándiz; Gabriela Guillena; Carmen Nájera
Journal:  Molecules       Date:  2015-07-16       Impact factor: 4.411

5.  Enantiodivergence by minimal modification of an acyclic chiral secondary aminocatalyst.

Authors:  Jun Dai; Zhuang Wang; Yuhua Deng; Lei Zhu; Fangzhi Peng; Yu Lan; Zhihui Shao
Journal:  Nat Commun       Date:  2019-11-15       Impact factor: 14.919
  5 in total

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