Results 31 to 40 of about 2,722 (150)

Enantioselective synthesis of chiral quinohelicenes through sequential organocatalyzed Povarov reaction and oxidative aromatization

open access: yesNature Communications, 2023
Heterohelicenes are of increasing importance in the fields of materials science, molecular recognition, and asymmetric catalysis. However, enantioselective construction of these molecules, especially by organocatalytic methods, is challenging, and few ...
Chengwen Li   +6 more
doaj   +1 more source

Chiral Phosphoric Acid Diesters as Ligands in Asymmetric Transition Metal Catalyzed Hydrogenation

open access: yesCHIMIA, 2003
A chiral phosphoric acid diester, specifically the BINOL-based derivative, has been used for the first time in Rh-, Ir-, and Pd-catalyzed hydrogenation of olefins and imines, giving ee-values of up to 85%.
Manfred T. Reetz   +2 more
doaj   +1 more source

Applications of chiral spirocyclic phosphoric acid in the synthesis of natural products [PDF]

open access: yesE3S Web of Conferences, 2021
With a 10 years development, chiral spirocyclic phosphoric acids (SPAs) have attracted a substantial amount of attention from the synthetic organic chemistry community. This kind of small molecule organic catalysts has some advantages like easy to obtain,
Yang Fan
doaj   +1 more source

Development of diverse adjustable axially chiral biphenyl ligands and catalysts

open access: yesiScience, 2023
Summary: Development of highly efficient and practical chiral ligands and catalysts is an eternal theme in asymmetric synthesis. Here, we report the design, synthesis, and evaluation of a new kind of adjustable axially chiral biphenyl ligands and ...
Jiyang Jie   +3 more
doaj   +1 more source

Organocatalytic asymmetric selenofunctionalization of tryptamine for the synthesis of hexahydropyrrolo[2,3-b]indole derivatives

open access: yesBeilstein Journal of Organic Chemistry, 2013
A chiral phosphoric acid-catalyzed selenofunctionalization of tryptamine derivatives provides access to 3a-(phenylselenyl)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole derivatives in high yields and with synthetically useful levels of enantioselectivity ...
Qiang Wei   +3 more
doaj   +1 more source

Organocatalytic asymmetric synthesis of bioactive hexahydropyrrolo[2,3-b]indole-containing tetrasubstituted allenes bearing multiple chiral elements

open access: yesTetrahedron Chem, 2022
An organocatalytic asymmetric construction of hexahydropyrrolo[2,3-b]indole-containing tetrasubstituted allene scaffolds bearing both axial chirality and central chirality has been established via a cascade 1,8-addition/dearomatization-cyclization ...
Jing-Yi Wang   +7 more
doaj   +1 more source

Highly Enantioselective Hydrogenation of Enamides Catalyzed by Chiral Phosphoric Acids [PDF]

open access: yesOrganic Letters, 2009
A highly enantioselective hydrogenation of enamides catalyzed by a dual chiral-achiral acid system was developed. By employing a substoichiometric amount of a chiral phosphoric acid and acetic acid, catalyst loadings as low as 1 mol % of the chiral catalyst were sufficient to provide excellent yield and enantioselectivity of the reduction product.
Guilong, Li, Jon C, Antilla
openaire   +2 more sources

Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination

open access: yesNature Communications, 2023
Planar chiral [2.2]paracyclophane derivatives are a type of structurally intriguing and practically useful chiral molecules, which have found a range of important applications in the field of asymmetric catalysis and material science.
Shaoze Yu   +3 more
doaj   +1 more source

Diastereo- and atroposelective synthesis of N-arylpyrroles enabled by light-induced phosphoric acid catalysis

open access: yesNature Communications, 2023
The C−N axially chiral N-arylpyrrole motifs are privileged scaffolds in numerous biologically active molecules and natural products, as well as in chiral ligands/catalysts.
Lei Dai   +5 more
doaj   +1 more source

Construction of Non-Biaryl Atropisomeric Amide Scaffolds Bearing a C–N Axis via Enantioselective Catalysis

open access: yesMolecules, 2022
The significant scaffold offered by atropisomeric amides with a C–N chiral axis has been extensively utilized for pharmaceuticals, agricultural science, and organic syntheses.
Xiao Xiao   +6 more
doaj   +1 more source

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