Literature DB >> 22505348

Rationally designed amide donors for organocatalytic asymmetric Michael reactions.

Bin Tan1, Gloria Hernández-Torres, Carlos F Barbas.   

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Year:  2012        PMID： 22505348     DOI： 10.1002/anie.201200996

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


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  5 in total

1.  Organocatalyzed asymmetric Michael reaction of β-aryl-α-ketophosphonates and nitroalkenes.

Authors:  Jie Guang; John Cong-Gui Zhao
Journal:  Tetrahedron Lett       Date:  2013-10-16       Impact factor: 2.415

2.  Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions.

Authors:  Alejandro Cabanillas; Christopher D Davies; Louise Male; Nigel S Simpkins
Journal:  Chem Sci       Date:  2014-11-28       Impact factor: 9.825

3.  Enantioselective Thiolysis and Aminolysis of Cyclic Anhydrides Using a Chiral Diamine-Derived Thiourea Catalyst.

Authors:  Jae Ho Shim; Sung Joo Park; Byung Kook Ahn; Ji Yeon Lee; Hyeon Soo Kim; Deok-Chan Ha
Journal:  ACS Omega       Date:  2021-11-24

4.  Enantioselective organocatalytic Michael reactions using chiral (R,R)-1,2-diphenylethylenediamine-derived thioureas.

Authors:  Jae Ho Shim; Min Ji Lee; Min Ho Lee; Byeong-Seon Kim; Deok-Chan Ha
Journal:  RSC Adv       Date:  2020-08-27       Impact factor: 4.036

5.  Synthesis of β-Hydroxy α-Amino Acids Through Brønsted Base-Catalyzed syn-Selective Direct Aldol Reaction of Schiff Bases of Glycine o-Nitroanilide.

Authors:  Silvia Vera; Ana Vázquez; Ricardo Rodriguez; Sandra Del Pozo; Iñaki Urruzuno; Abel de Cózar; Antonia Mielgo; Claudio Palomo
Journal:  J Org Chem       Date:  2021-05-16       Impact factor: 4.198
  5 in total

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