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Bažina Systematicky mramor palladium ii catalyzed claisen rearrangement Potrubí Ru Koza

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

A continuous-flow resonator-type microwave reactor for high-efficiency organic synthesis and Claisen rearrangement as a model re
A continuous-flow resonator-type microwave reactor for high-efficiency organic synthesis and Claisen rearrangement as a model re

Claisen Rearrangement
Claisen Rearrangement

The Allylic Trihaloacetimidate Rearrangement - Overman - - Major Reference Works - Wiley Online Library
The Allylic Trihaloacetimidate Rearrangement - Overman - - Major Reference Works - Wiley Online Library

Pd(II)-catalyzed aliphatic Claisen rearrangements of acyclic allyl vinyl ethers - ScienceDirect
Pd(II)-catalyzed aliphatic Claisen rearrangements of acyclic allyl vinyl ethers - ScienceDirect

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

Carroll rearrangement - Wikipedia
Carroll rearrangement - Wikipedia

Top PDF Concerning the mechanism and selectivity of palladium(II)-catalyzed aerobic oxidation reactions - 1Library
Top PDF Concerning the mechanism and selectivity of palladium(II)-catalyzed aerobic oxidation reactions - 1Library

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

Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram
Proposed mechanism for Pd-catalysed rearrangement of allyloxypurines I. | Download Scientific Diagram

Molecules | Free Full-Text | Pd(II)-Catalyzed C-H Acylation of (Hetero)arenes—Recent Advances | HTML
Molecules | Free Full-Text | Pd(II)-Catalyzed C-H Acylation of (Hetero)arenes—Recent Advances | HTML

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

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

Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides | Nature Communications
Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides | Nature Communications

Pd(II)-catalyzed aliphatic Claisen rearrangements of acyclic allyl vinyl ethers - ScienceDirect
Pd(II)-catalyzed aliphatic Claisen rearrangements of acyclic allyl vinyl ethers - ScienceDirect

Claisen Rearrangement
Claisen Rearrangement

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

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

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)

Molecules | Free Full-Text | Focusing on the Catalysts of the Pd- and Ni- Catalyzed Hirao Reactions | HTML
Molecules | Free Full-Text | Focusing on the Catalysts of the Pd- and Ni- Catalyzed Hirao Reactions | HTML

Enantioselective catalysis of Claisen rearrangement by DABNTf–Pd(II) complex - ScienceDirect
Enantioselective catalysis of Claisen rearrangement by DABNTf–Pd(II) complex - ScienceDirect

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

Palladium catalyzed polyhetero-Claisen rearrangement - [PDF Document]
Palladium catalyzed polyhetero-Claisen rearrangement - [PDF Document]

A gold-catalysed enantioselective Cope rearrangement of achiral 1,5-dienes | Nature Chemistry
A gold-catalysed enantioselective Cope rearrangement of achiral 1,5-dienes | Nature Chemistry

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

Reductive Iodonium: Teaching an Old Claisen New Tricks: Trends in Chemistry
Reductive Iodonium: Teaching an Old Claisen New Tricks: Trends in Chemistry

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