Literature DB >> 21958056

N-Prolinylanthranilamide pseudopeptides as bifunctional organocatalysts for asymmetric aldol reactions.

Anthony J Pearson1, Santanu Panda.   

Abstract

Proline anthranilamide-based pseudopeptides were shown to be effective organocatalysts for enantioselective direct aldol reactions of a selection of aldehydes with various ketones with excellent yield, enantioselectivity up to 99% and anti to syn diastereoselectivity up to 25:1.
© 2011 American Chemical Society

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Year:  2011        PMID： 21958056     DOI： 10.1021/ol202284n

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


  2 in total

1.  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

2.  Cu(ii)-thiophene-2,5-bis(amino-alcohol) mediated asymmetric Aldol reaction and Domino Knoevenagel Michael cyclization: a new highly efficient Lewis acid catalyst.

Authors:  Abdullah Mohammed Al-Majid; Abdullah Saleh Alammari; Saeed Alshahrani; Matti Haukka; Mohammad Shahidul Islam; Assem Barakat
Journal:  RSC Adv       Date:  2022-02-21       Impact factor: 3.361
  2 in total

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