Literature DB >> 19178161

Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins.

Bukuo Ni1, Qianying Zhang, Kritanjali Dhungana, Allan D Headley.   

Abstract

A new class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst has been developed and shown to be a very effective catalyst for the asymmetric Michael addition reactions of ketones and aldehyde to nitroolefins with high enantio- and diastereoselectivities. This ILS organocatalyst is also easily recycled and could be reused at least five times without significant loss of its ability to affect the outcome of the asymmetric reactions.

Entities:  

Year:  2009        PMID: 19178161     DOI: 10.1021/ol900003e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Exploring a sulfone linker utilizing trimethyl aluminum as a cleavage reagent: solid-phase synthesis of sulfonamides and ureas.

Authors:  Tsai-Wen Chung; Chih-Hau Chen; Chu-Chung Lin; Hsien-Jen Wu; Chung-Ming Sun; Wen-Sheng Chung
Journal:  Mol Divers       Date:  2012-06-30       Impact factor: 2.943

2.  Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation.

Authors:  J Tůma; M Kohout
Journal:  RSC Adv       Date:  2018-01-03       Impact factor: 4.036

Review 3.  Asymmetric Michael Addition Mediated by Chiral Ionic Liquids.

Authors:  Yumiko Suzuki
Journal:  Mini Rev Org Chem       Date:  2018-06       Impact factor: 2.495

  3 in total

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