![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
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Diastereocontrol via the phenol- and palladium(II)-catalyzed Claisen rearrangement with cyclic enol ethers - ScienceDirect
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Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)
![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
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Asymmetric Synthesis of Allenyl Oxindoles and Spirooxindoles by a Catalytic Enantioselective Saucy–Marbet Claisen Rearrangement - Cao - 2012 - Angewandte Chemie International Edition - Wiley Online Library
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Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. - Abstract - Europe PMC
Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles - Chemical Communications (RSC Publishing)
A continuous-flow resonator-type microwave reactor for high-efficiency organic synthesis and Claisen rearrangement as a model re
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Top PDF Concerning the mechanism and selectivity of palladium(II)-catalyzed aerobic oxidation reactions - 1Library
![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
![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
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Copper(II)- and Palladium(II)-Catalyzed Enantioselective Claisen Rearrangement of Allyloxy- and Propargyloxy-Indoles
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