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A Dearomatization/Debromination Strategy for the [4+1] Spiroannulation of Bromophenols with α,β‐Unsaturated Imines.
- Published in:
- Angewandte Chemie, 2020, v. 132, n. 43, p. 19147, doi. 10.1002/ange.202008130
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- Article
Palladium‐Catalyzed [2+2+1] Spiroannulation via Alkyne‐Directed Remote C−H Arylation and Subsequent Arene Dearomatization.
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- Angewandte Chemie, 2020, v. 132, n. 2, p. 663, doi. 10.1002/ange.201909557
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- Article
Palladium‐Catalyzed Intermolecular [4+1] Spiroannulation by C(sp<sup>3</sup>)−H Activation and Naphthol Dearomatization.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1488, doi. 10.1002/ange.201813202
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- Article
Palladium/Norbornene‐Catalyzed C−H Alkylation/Alkyne Insertion/Indole Dearomatization Domino Reaction: Assembly of Spiroindolenine‐Containing Pentacyclic Frameworks.
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- Angewandte Chemie, 2018, v. 130, n. 18, p. 5245, doi. 10.1002/ange.201801894
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- Article
Rapid Assembly of Diversely Functionalized Spiroindenes by a Three-Component Palladium-Catalyzed C−H Amination/Phenol Dearomatization Domino Reaction.
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- Angewandte Chemie, 2017, v. 129, n. 45, p. 14445, doi. 10.1002/ange.201708310
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- Article
Modular Assembly of Spirocarbocyclic Scaffolds through Pd<sup>0</sup>-Catalyzed Intermolecular Dearomatizing [2+2+1] Annulation of Bromonaphthols with Aryl Iodides and Alkynes.
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- Angewandte Chemie, 2017, v. 129, n. 10, p. 2811, doi. 10.1002/ange.201612127
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- Article
Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1, n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds.
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- Angewandte Chemie, 2016, v. 128, n. 24, p. 7060, doi. 10.1002/ange.201601570
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- Article
[3+2] Cycloaddition of Vinyl Cyclopropane and Hydroxylamines via Isocynate Intermediate to γ‐Lactams.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 16, p. 1937, doi. 10.1002/cjoc.202300008
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- Article
Trifunctionalization of Aryl Iodides with Two Distinct Nitrogen and Carbon Electrophiles by Palladium/Norbornene Catalysis.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 10, p. 2659, doi. 10.1002/cjoc.202100467
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- Article
Catellani Reaction: An Enabling Technology for Vicinal Functionalization of Aryl Halides by Palladium(0)/Norbornene Cooperative Catalysis.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 6, p. 1690, doi. 10.1002/cjoc.202000600
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- Article
Palladium‐Catalyzed Intermolecular [4+1] Spiroannulation by C(sp<sup>3</sup>)−H Activation and Naphthol Dearomatization.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 5, p. 1474, doi. 10.1002/anie.201813202
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- Publication type:
- Article
Palladium/Norbornene-Catalyzed C-H Alkylation/Alkyne Insertion/ Indole Dearomatization Domino Reaction: Assembly of Spiroindolenine-Containing Pentacyclic Frameworks.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 18, p. 5151, doi. 10.1002/anie.201801894
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- Publication type:
- Article
Rapid Assembly of Diversely Functionalized Spiroindenes by a Three-Component Palladium-Catalyzed C−H Amination/Phenol Dearomatization Domino Reaction.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 45, p. 14257, doi. 10.1002/anie.201708310
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- Publication type:
- Article
Modular Assembly of Spirocarbocyclic Scaffolds through Pd<sup>0</sup>-Catalyzed Intermolecular Dearomatizing [2+2+1] Annulation of Bromonaphthols with Aryl Iodides and Alkynes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 10, p. 2767, doi. 10.1002/anie.201612127
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- Publication type:
- Article
Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1, n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 24, p. 6946, doi. 10.1002/anie.201601570
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- Article
Highly Stereoselective Synthesis of Imine-Containing Dibenzo- [b,d]azepines by a Palladium(II)-Catalyzed [5+2] Oxidative Annulation of o-Arylanilines with Alkynes.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 51, p. 15385, doi. 10.1002/anie.201508850
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- Article
Direct Asymmetric Dearomatization of 2-Naphthols by Scandium-Catalyzed Electrophilic Amination.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 8, p. 2356, doi. 10.1002/anie.201409565
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- Article
Highly Stereoselective Synthesis of Imine-Containing Dibenzo[b,d]azepines by a Palladium(II)-Catalyzed [5+2] Oxidative Annulation of o-Arylanilines with Alkynes.
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- Angewandte Chemie, 2015, v. 127, n. 51, p. 15605, doi. 10.1002/ange.201508850
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- Article
Direct Asymmetric Dearomatization of 2-Naphthols by Scandium-Catalyzed Electrophilic Amination.
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- Angewandte Chemie, 2015, v. 127, n. 8, p. 2386, doi. 10.1002/ange.201409565
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- Article
Cooperative Photoredox and Cobalt‐Catalyzed Acceptorless Dehydrogenative Functionalization of Cyclopropylamides towards Allylic N,O‐Acyl‐acetal Derivatives.
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- Angewandte Chemie, 2024, v. 136, n. 24, p. 1, doi. 10.1002/ange.202401579
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- Article
Selective C(sp<sup>3</sup>)−N Bond Cleavage of N,N‐Dialkyl Tertiary Amines with the Loss of a Large Alkyl Group via an S<sub>N</sub>1 Pathway.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202113820
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- Article
Cooperative Photoredox and Cobalt‐Catalyzed Acceptorless Dehydrogenative Functionalization of Cyclopropylamides towards Allylic N,O‐Acyl‐acetal Derivatives.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 24, p. 1, doi. 10.1002/anie.202401579
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- Publication type:
- Article
Selective C(sp<sup>3</sup>)−N Bond Cleavage of N,N‐Dialkyl Tertiary Amines with the Loss of a Large Alkyl Group via an S<sub>N</sub>1 Pathway.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 3, p. 1, doi. 10.1002/anie.202113820
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- Publication type:
- Article
A Dearomatization/Debromination Strategy for the [4+1] Spiroannulation of Bromophenols with α,β‐Unsaturated Imines.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 43, p. 18985, doi. 10.1002/anie.202008130
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- Publication type:
- Article
Palladium‐Catalyzed [2+2+1] Spiroannulation via Alkyne‐Directed Remote C−H Arylation and Subsequent Arene Dearomatization.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 2, p. 653, doi. 10.1002/anie.201909557
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- Publication type:
- Article
Unprecedented Selectivity via Electronic Substrate Recognition in the 1,4-Addition to Cyclic Olefins Using a Chiral Disulfoxide Rhodium Catalyst.
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- Angewandte Chemie, 2009, v. 121, n. 15, p. 2806, doi. 10.1002/ange.200900429
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- Article
C<sub>2</sub>-Symmetric Chiral Disulfoxide Ligands in Rhodium-Catalyzed 1,4-Addition: From Ligand Synthesis to the Enantioselection Pathway.
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- Chemistry - A European Journal, 2010, v. 16, n. 48, p. 14335, doi. 10.1002/chem.201001749
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- Article
Unprecedented Selectivity via Electronic Substrate Recognition in the 1,4-Addition to Cyclic Olefins Using a Chiral Disulfoxide Rhodium Catalyst.
- Published in:
- Angewandte Chemie International Edition, 2009, v. 48, n. 15, p. 2768, doi. 10.1002/anie.200900429
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- Article