![Table 1.4 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar Table 1.4 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar](https://ai2-s2-public.s3.amazonaws.com/figures/2017-08-08/a28022adaf181cc57b3e00b3793965b24745aa72/25-Table1.4-1.png)
Table 1.4 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar
![Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. - Abstract - Europe PMC Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. - Abstract - Europe PMC](https://europepmc.org/articles/PMC4030764/bin/nihms-582830-f0022.jpg)
Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. - Abstract - Europe PMC
![A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B501346C A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B501346C](https://pubs.rsc.org/image/article/2005/OB/b501346c/b501346c-s1.gif)
A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B501346C
![Regiochemical control in the Pd(II)-catalyzed claisen rearrangement via in situ enol ether exchange - ScienceDirect Regiochemical control in the Pd(II)-catalyzed claisen rearrangement via in situ enol ether exchange - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-004040399601790X-gr1.gif)
Regiochemical control in the Pd(II)-catalyzed claisen rearrangement via in situ enol ether exchange - ScienceDirect
![Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a28022adaf181cc57b3e00b3793965b24745aa72/96-Table2.2-1.png)
Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar
![Diastereocontrol via the phenol- and palladium(II)-catalyzed Claisen rearrangement with cyclic enol ethers - ScienceDirect Diastereocontrol via the phenol- and palladium(II)-catalyzed Claisen rearrangement with cyclic enol ethers - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403901810790-gr1.gif)
Diastereocontrol via the phenol- and palladium(II)-catalyzed Claisen rearrangement with cyclic enol ethers - ScienceDirect
![PDF) A new palladium(II)-catalyzed [3,3] aza-Claisen rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles | Antonio Piccionello - Academia.edu PDF) A new palladium(II)-catalyzed [3,3] aza-Claisen rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles | Antonio Piccionello - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/44982140/mini_magick20190213-14539-zxuyqy.png?1550072610)
PDF) A new palladium(II)-catalyzed [3,3] aza-Claisen rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles | Antonio Piccionello - Academia.edu
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Molecules | Free Full-Text | Pd(II)-Catalyzed C-H Acylation of (Hetero)arenes—Recent Advances | HTML
![Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing) Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)](https://pubs.rsc.org/image/article/2020/cc/d0cc04590j/d0cc04590j-s1_hi-res.gif)
Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)
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Top PDF Concerning the mechanism and selectivity of palladium(II)-catalyzed aerobic oxidation reactions - 1Library
![Table 1.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar Table 1.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a28022adaf181cc57b3e00b3793965b24745aa72/23-Table1.2-1.png)
Table 1.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar
![Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram](https://www.researchgate.net/profile/Hana_Dvorakova/publication/257908940/figure/fig2/AS:668996705718290@1536512652768/Proposed-mechanism-for-Pd-catalysed-rearrangement-of-allyloxypurines-I.png)
Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram
![Figure 1.2 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar Figure 1.2 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a28022adaf181cc57b3e00b3793965b24745aa72/14-Figure1.2-1.png)
Figure 1.2 from Part A: Palladium(II)-catalyzed enantioselective Saucy-Marbet Claisen rearrangement of propargyloxy indoles to quaternary oxindoles and spirocyclic lactones. Part B: The regioselective oxidative coupling of phenols | Semantic Scholar
![Table 2.5 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar Table 2.5 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar](https://ai2-s2-public.s3.amazonaws.com/figures/2017-08-08/a28022adaf181cc57b3e00b3793965b24745aa72/108-Table2.5-1.png)
Table 2.5 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar
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Copper(II)- and Palladium(II)-Catalyzed Enantioselective Claisen Rearrangement of Allyloxy- and Propargyloxy-Indoles
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The Allylic Trihaloacetimidate Rearrangement - Overman - - Major Reference Works - Wiley Online Library
![Tandem Pd(II)-Catalyzed Vinyl Ether Exchange−Claisen Rearrangement as a Facile Approach to γ,δ-Unsaturated Aldehydes Tandem Pd(II)-Catalyzed Vinyl Ether Exchange−Claisen Rearrangement as a Facile Approach to γ,δ-Unsaturated Aldehydes](https://s3-eu-west-1.amazonaws.com/ppreviews-acs-4898564/4706413/thumb.png)
Tandem Pd(II)-Catalyzed Vinyl Ether Exchange−Claisen Rearrangement as a Facile Approach to γ,δ-Unsaturated Aldehydes
![Molecules | Free Full-Text | Pd(II)/HPMoV-Catalyzed Direct Oxidative Coupling Reaction of Benzenes with Olefins | HTML Molecules | Free Full-Text | Pd(II)/HPMoV-Catalyzed Direct Oxidative Coupling Reaction of Benzenes with Olefins | HTML](https://www.mdpi.com/molecules/molecules-15-01487/article_deploy/html/images/molecules-15-01487-sch001.png)
Molecules | Free Full-Text | Pd(II)/HPMoV-Catalyzed Direct Oxidative Coupling Reaction of Benzenes with Olefins | HTML
![Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar](https://ai2-s2-public.s3.amazonaws.com/figures/2017-08-08/a28022adaf181cc57b3e00b3793965b24745aa72/13-Figure1.1-1.png)
Table 2.2 from Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . | Semantic Scholar
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Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. - Abstract - Europe PMC
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