Literature DB >> 35080408

Enantioselective Pictet-Spengler Reaction of Acyclic α-Ketoesters Using Chiral Imidazoline-Phosphoric Acid Catalysts.

Shuichi Nakamura1,2, Yoichiro Matsuda2, Tsunayoshi Takehara3, Takeyuki Suzuki3.   

Abstract

The first enantioselective Pictet-Spengler reaction of acyclic α-ketoesters with tryptamines has been developed. Excellent yields and enantioselectivity were obtained for the reaction using chiral imidazoline-phosphoric acid catalysts. Density functional theory calculations suggested possible transition states that explain the origin of chiral induction. This process provides an efficient route for the synthesis of tetrahydro-β-carboline derivatives.

Entities:  

Year:  2022        PMID: 35080408     DOI: 10.1021/acs.orglett.1c04316

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


  2 in total

1.  Screening for generality in asymmetric catalysis.

Authors:  Corin C Wagen; Spencer E McMinn; Eugene E Kwan; Eric N Jacobsen
Journal:  Nature       Date:  2022-09-01       Impact factor: 69.504

2.  Catalytic Enantioselective Pictet-Spengler Reaction of α-Ketoamides Catalyzed by a Single H-Bond Donor Organocatalyst.

Authors:  Rémi Andres; Qian Wang; Jieping Zhu
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-11       Impact factor: 16.823

  2 in total

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