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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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Tandem Pd(II)-Catalyzed Vinyl Ether Exchange−Claisen Rearrangement as a Facile Approach to γ,δ-Unsaturated Aldehydes
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Copper(II)- and Palladium(II)-Catalyzed Enantioselective Claisen Rearrangement of Allyloxy- and Propargyloxy-Indoles
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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
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The Allylic Trihaloacetimidate Rearrangement - Overman - - Major Reference Works - Wiley Online Library
![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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Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram
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Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)
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Regiochemical control in the Pd(II)-catalyzed claisen rearrangement via in situ enol ether exchange - ScienceDirect
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Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)
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Molecules | Free Full-Text | Focusing on the Catalysts of the Pd- and Ni- Catalyzed Hirao Reactions | HTML
![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)