Literature DB >> 26083993

Organocatalytic enantioselective formal arylation of azlactones using quinones as the aromatic partner.

Guofeng Li1, Wangsheng Sun, Jingyi Li, Fengjing Jia, Liang Hong, Rui Wang.   

Abstract

A new method for the catalytic enantioselective formal arylation of azlactones using quinones as the aromatic partner was developed for the first time. Under mild conditions, the domino Michael/aromatization/cyclization reaction worked well to afford the corresponding products in moderate to high yields with excellent enantioselectivities, some of which have promising cytotoxicity against cancer cells and antibacterial activities.

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Year:  2015        PMID: 26083993     DOI: 10.1039/c5cc03677a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Diastereoselective synthesis of vicinal tertiary and N-substituted quaternary stereogenic centers by catalytic hydroalkylation of dienes.

Authors:  Matthew J Goldfogel; Simon J Meek
Journal:  Chem Sci       Date:  2016-03-11       Impact factor: 9.825

Review 2.  Naphthoquinone Tryptophan Hybrids: A Promising Small Molecule Scaffold for Mitigating Aggregation of Amyloidogenic Proteins and Peptides.

Authors:  Guru KrishnaKumar Viswanathan; Ashim Paul; Ehud Gazit; Daniel Segal
Journal:  Front Cell Dev Biol       Date:  2019-10-17
  2 in total

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