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Palladium-Catalyzed Enantioselective C-3 Allylation of 3-Substituted-1H- Indoles Using Trialkylboranes | Journal of the American Chemical Society
Palladium-Catalyzed Enantioselective C-3 Allylation of 3-Substituted-1H- Indoles Using Trialkylboranes | Journal of the American Chemical Society

Palladium-Catalyzed Enantioselective C-3 Allylation of 3-Substituted-1H- Indoles Using Trialkylboranes | Journal of the American Chemical Society
Palladium-Catalyzed Enantioselective C-3 Allylation of 3-Substituted-1H- Indoles Using Trialkylboranes | Journal of the American Chemical Society

Molecules | Free Full-Text | Recent Advances in the Synthesis of 3,n-Fused  Tricyclic Indole Skeletons via Palladium-Catalyzed Domino Reactions
Molecules | Free Full-Text | Recent Advances in the Synthesis of 3,n-Fused Tricyclic Indole Skeletons via Palladium-Catalyzed Domino Reactions

Palladium-catalyzed regio- and enantioselective migratory allylic C(sp3)-H  functionalization | Nature Communications
Palladium-catalyzed regio- and enantioselective migratory allylic C(sp3)-H functionalization | Nature Communications

Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation  of Internal Alkynes | The Journal of Organic Chemistry
Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation of Internal Alkynes | The Journal of Organic Chemistry

Palladium-Catalyzed Asymmetric Allylic Alkylation/α-Iminol Rearrangement: A  Facile Access to 2-Spirocyclic-Indoline Derivatives | CCS Chemistry
Palladium-Catalyzed Asymmetric Allylic Alkylation/α-Iminol Rearrangement: A Facile Access to 2-Spirocyclic-Indoline Derivatives | CCS Chemistry

Pd-Catalyzed C3-Selective Allylation of Indoles with Allyl Alcohols  Promoted by Triethylborane | Journal of the American Chemical Society
Pd-Catalyzed C3-Selective Allylation of Indoles with Allyl Alcohols Promoted by Triethylborane | Journal of the American Chemical Society

Application of the Asymmetric Pictet-Spengler Reaction in the Total  Synthesis of Natural Products and Relevant Biologically Active Compounds. -  Abstract - Europe PMC
Application of the Asymmetric Pictet-Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds. - Abstract - Europe PMC

The Palladium Catalyzed Asymmetric Addition of Oxindoles and Allenes: An  Atom-Economical Versatile Method for the Construction of Chiral Indole  Alkaloids | Journal of the American Chemical Society
The Palladium Catalyzed Asymmetric Addition of Oxindoles and Allenes: An Atom-Economical Versatile Method for the Construction of Chiral Indole Alkaloids | Journal of the American Chemical Society

Palladium-catalyzed synthesis of 3-alkoxysubstituted indoles - ScienceDirect
Palladium-catalyzed synthesis of 3-alkoxysubstituted indoles - ScienceDirect

Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler  Reaction in the Total Synthesis of Natural Products and Relevant  Biologically Active Compounds
Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation  of Internal Alkynes | The Journal of Organic Chemistry
Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation of Internal Alkynes | The Journal of Organic Chemistry

Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler  Reaction in the Total Synthesis of Natural Products and Relevant  Biologically Active Compounds
Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Synthesis of 3-acylindoles by palladium-catalyzed acylation of free (N-H)  indoles with nitriles. | Semantic Scholar
Synthesis of 3-acylindoles by palladium-catalyzed acylation of free (N-H) indoles with nitriles. | Semantic Scholar

Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler  Reaction in the Total Synthesis of Natural Products and Relevant  Biologically Active Compounds
Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Application of the Asymmetric Pictet-Spengler Reaction in the Total  Synthesis of Natural Products and Relevant Biologically Active Compounds. -  Abstract - Europe PMC
Application of the Asymmetric Pictet-Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds. - Abstract - Europe PMC

Application of the Asymmetric Pictet-Spengler Reaction in the Total  Synthesis of Natural Products and Relevant Biologically Active Compounds. -  Abstract - Europe PMC
Application of the Asymmetric Pictet-Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds. - Abstract - Europe PMC

Palladium-catalyzed synthesis of 3-alkoxysubstituted indoles - ScienceDirect
Palladium-catalyzed synthesis of 3-alkoxysubstituted indoles - ScienceDirect

Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation  of Internal Alkynes | The Journal of Organic Chemistry
Synthesis of 2,3-Disubstituted Indoles via Palladium-Catalyzed Annulation of Internal Alkynes | The Journal of Organic Chemistry

Palladium-catalyzed carbonylative cyclization of alkene-tethered indoles  with phenols or arylboronic acids: Construction of carbonyl-containing  indolo[2,1-a]isoquinoline derivatives
Palladium-catalyzed carbonylative cyclization of alkene-tethered indoles with phenols or arylboronic acids: Construction of carbonyl-containing indolo[2,1-a]isoquinoline derivatives

Palladium-Catalyzed β-Allylation of 2,3-Disubstituted Indoles | Organic  Letters
Palladium-Catalyzed β-Allylation of 2,3-Disubstituted Indoles | Organic Letters

PDF) Application of the Asymmetric Pictet–Spengler Reaction in the Total  Synthesis of Natural Products and Relevant Biologically Active Compounds
PDF) Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler  Reaction in the Total Synthesis of Natural Products and Relevant  Biologically Active Compounds
Molecules | Free Full-Text | Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds

Catalytic asymmetric dipolar cycloadditions of indolyl delocalized  metal-allyl species for the enantioselective synthesis of cyclopenta [b] indoles and pyrrolo[1,2-a]indoles | Science China Chemistry
Catalytic asymmetric dipolar cycloadditions of indolyl delocalized metal-allyl species for the enantioselective synthesis of cyclopenta [b] indoles and pyrrolo[1,2-a]indoles | Science China Chemistry