![Synthesis of tetra-substituted 5-trifluoromethylpyrazoles via sequential halogenation/palladium-catalyzed C–C and C–N cross-coupling - Organic & Biomolecular Chemistry (RSC Publishing) Synthesis of tetra-substituted 5-trifluoromethylpyrazoles via sequential halogenation/palladium-catalyzed C–C and C–N cross-coupling - Organic & Biomolecular Chemistry (RSC Publishing)](https://pubs.rsc.org/image/article/2016/ob/c5ob02390d/c5ob02390d-u1_hi-res.gif)
Synthesis of tetra-substituted 5-trifluoromethylpyrazoles via sequential halogenation/palladium-catalyzed C–C and C–N cross-coupling - Organic & Biomolecular Chemistry (RSC Publishing)
![Ubiquitous Benzoquinones, Multitalented Compounds for Palladium‐Catalyzed Oxidative Reactions - Vasseur - 2015 - European Journal of Organic Chemistry - Wiley Online Library Ubiquitous Benzoquinones, Multitalented Compounds for Palladium‐Catalyzed Oxidative Reactions - Vasseur - 2015 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/333420bb-a853-4e84-baf9-d2b2d140293a/mfig000.jpg)
Ubiquitous Benzoquinones, Multitalented Compounds for Palladium‐Catalyzed Oxidative Reactions - Vasseur - 2015 - European Journal of Organic Chemistry - Wiley Online Library
![Tunable synthesis of quinolinone-fused isoquinolines through sequential one-pot nucleophilic addition and palladium-catalyzed intramolecular C–H alken ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02437E Tunable synthesis of quinolinone-fused isoquinolines through sequential one-pot nucleophilic addition and palladium-catalyzed intramolecular C–H alken ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02437E](https://pubs.rsc.org/image/article/2019/OB/c8ob02437e/c8ob02437e-s1_hi-res.gif)
Tunable synthesis of quinolinone-fused isoquinolines through sequential one-pot nucleophilic addition and palladium-catalyzed intramolecular C–H alken ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02437E
![PDF) 1,4-Palladium Shift/C(sp 3 )–H Activation Strategy for the Remote Construction of Five-Membered Rings PDF) 1,4-Palladium Shift/C(sp 3 )–H Activation Strategy for the Remote Construction of Five-Membered Rings](https://i1.rgstatic.net/publication/330978937_14-Palladium_ShiftCsp_3_-H_Activation_Strategy_for_the_Remote_Construction_of_Five-Membered_Rings/links/5d1f0deaa6fdcc2462c11ccb/largepreview.png)
PDF) 1,4-Palladium Shift/C(sp 3 )–H Activation Strategy for the Remote Construction of Five-Membered Rings
![3-(2-Alken-1-one-2-yl)indoles through the palladium-catalyzed reaction of 2-alkynyltrifluoroacetanilides with cyclic α-iodoenones - ScienceDirect 3-(2-Alken-1-one-2-yl)indoles through the palladium-catalyzed reaction of 2-alkynyltrifluoroacetanilides with cyclic α-iodoenones - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402010001559-sc1.jpg)
3-(2-Alken-1-one-2-yl)indoles through the palladium-catalyzed reaction of 2-alkynyltrifluoroacetanilides with cyclic α-iodoenones - ScienceDirect
![PDF) Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes | Adriano Vieira - Academia.edu PDF) Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes | Adriano Vieira - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/46178124/mini_magick20190210-28218-dy44ii.png?1549819072)
PDF) Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes | Adriano Vieira - Academia.edu
![PDF) Palladium-Catalyzed Cross-Coupling of Aryl and Alkenyl Boronic Acids with Alkenes via Oxidative Addition of a Carbon-Boron Bond to Palladium(0) PDF) Palladium-Catalyzed Cross-Coupling of Aryl and Alkenyl Boronic Acids with Alkenes via Oxidative Addition of a Carbon-Boron Bond to Palladium(0)](https://i1.rgstatic.net/publication/222879486_Palladium-Catalyzed_Cross-Coupling_of_Aryl_and_Alkenyl_Boronic_Acids_with_Alkenes_via_Oxidative_Addition_of_a_Carbon-Boron_Bond_to_Palladium0/links/5b2c426d0f7e9b0df5ba52eb/largepreview.png)
PDF) Palladium-Catalyzed Cross-Coupling of Aryl and Alkenyl Boronic Acids with Alkenes via Oxidative Addition of a Carbon-Boron Bond to Palladium(0)
![Synthesis and functionalization of indoles through palladium-catalyzed reactions. | Semantic Scholar Synthesis and functionalization of indoles through palladium-catalyzed reactions. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/6b914ea9fc2c69aa88223cd2ad49740963ab8867/5-Figure2-1.png)
Synthesis and functionalization of indoles through palladium-catalyzed reactions. | Semantic Scholar
![Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives](https://reader021.docslide.net/reader021/html5/20170820/575021a31a28ab877ea0c880/bg2.png)
Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives
![Palladium-Catalyzed Four-Component Cascade Reaction for the Synthesis of Highly Functionalized Acyclic O,O-Acetals - Org. Lett. - X-MOL Palladium-Catalyzed Four-Component Cascade Reaction for the Synthesis of Highly Functionalized Acyclic O,O-Acetals - Org. Lett. - X-MOL](https://xpic.x-mol.com/20180118%2F10.1021_acs.orglett.7b03808.jpg)
Palladium-Catalyzed Four-Component Cascade Reaction for the Synthesis of Highly Functionalized Acyclic O,O-Acetals - Org. Lett. - X-MOL
![Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives](https://reader021.docslide.net/reader021/html5/20170820/575021a31a28ab877ea0c880/bg1.png)
Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of E-4-amino-2-alken-1-ol derivatives
![PDF) The Role of Palladium Catalyst and Base in Stereoselective Transformations of (E)-2-Chlorovinylsulfides. PDF) The Role of Palladium Catalyst and Base in Stereoselective Transformations of (E)-2-Chlorovinylsulfides.](https://i1.rgstatic.net/publication/232376742_The_Role_of_Palladium_Catalyst_and_Base_in_Stereoselective_Transformations_of_E-2-Chlorovinylsulfides/links/5a2a52cbaca2728e05db24e9/largepreview.png)
PDF) The Role of Palladium Catalyst and Base in Stereoselective Transformations of (E)-2-Chlorovinylsulfides.
![PDF) Synthesis of Symmetrical and Unsymmetrical Diarylalkynes from Propiolic Acid Using Palladium-Catalyzed Decarboxylative Coupling | Sunwoo Lee - Academia.edu PDF) Synthesis of Symmetrical and Unsymmetrical Diarylalkynes from Propiolic Acid Using Palladium-Catalyzed Decarboxylative Coupling | Sunwoo Lee - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/31706202/mini_magick20190426-32177-1iqhf7.png?1556263264)
PDF) Synthesis of Symmetrical and Unsymmetrical Diarylalkynes from Propiolic Acid Using Palladium-Catalyzed Decarboxylative Coupling | Sunwoo Lee - Academia.edu
![Palladium-catalyzed trans-selective alkynylation–alkylation tandem process for the synthesis of (E)-3-alkyl-1-trialkylsilyl-3-alken-1-ynes - ScienceDirect Palladium-catalyzed trans-selective alkynylation–alkylation tandem process for the synthesis of (E)-3-alkyl-1-trialkylsilyl-3-alken-1-ynes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402005013335-gr1.gif)
Palladium-catalyzed trans-selective alkynylation–alkylation tandem process for the synthesis of (E)-3-alkyl-1-trialkylsilyl-3-alken-1-ynes - ScienceDirect
![Rapid assembly of 3-azidomethylfurans from 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis,Tetrahedron - X-MOL Rapid assembly of 3-azidomethylfurans from 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis,Tetrahedron - X-MOL](https://xpic.x-mol.com/20200627%2F10.1016_j.tet.2020.131327.jpg)
Rapid assembly of 3-azidomethylfurans from 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis,Tetrahedron - X-MOL
![PDF) Binuclear palladium(I) and platinum(I) dimers stabilized by aromatic ligands: Synthesis, structural characterization and reactivity with carbon monoxide PDF) Binuclear palladium(I) and platinum(I) dimers stabilized by aromatic ligands: Synthesis, structural characterization and reactivity with carbon monoxide](https://i1.rgstatic.net/publication/239221290_Binuclear_palladiumI_and_platinumI_dimers_stabilized_by_aromatic_ligands_Synthesis_structural_characterization_and_reactivity_with_carbon_monoxide/links/57b6ee1008aea2f4aec38429/largepreview.png)
PDF) Binuclear palladium(I) and platinum(I) dimers stabilized by aromatic ligands: Synthesis, structural characterization and reactivity with carbon monoxide
![PDF) The effect of added silver nitrate on the palladium-catalyzed arylation of allyltrimethylsilanes PDF) The effect of added silver nitrate on the palladium-catalyzed arylation of allyltrimethylsilanes](https://i1.rgstatic.net/publication/231577693_The_effect_of_added_silver_nitrate_on_the_palladium-catalyzed_arylation_of_allyltrimethylsilanes/links/5aaf60a30f7e9b4897c03f8a/largepreview.png)