ReviewBeilstein journal of organic chemistry2013
New developments in gold-catalyzed manipulation of inactivated alkenes.
Review in Beilstein journal of organic chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
9 citing papers in PubMed.
- Dicoordinate Au(I)-Ethylene Complexes as Hydroamination Catalysts.ACS catalysis · 2022Article
- Methodologies for the synthesis of quaternary carbon centers via hydroalkylation of unactivated olefins: twenty years of advances.Beilstein journal of organic chemistry · 2021Review
- Gold Redox Catalysis with a Selenium Cation as a Mild Oxidant.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
- Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes.Chemical science · 2020Article
- Allenes and Derivatives in Gold(I)- and Platinum(II)-Catalyzed Formal Cycloadditions.Accounts of chemical research · 2019Article
- Gold-Catalyzed Addition of β-Ketoesters to Alkenes: Influence of Electronic and Steric Effects in the Reaction Outcome.Molecules (Basel, Switzerland) · 2018Article
- Gold Redox Catalysis through Base-Initiated Diazonium Decomposition toward Alkene, Alkyne, and Allene Activation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017Article
- Controlled Interconversion of a Dinuclear Au Species Supported by a Redox-Active Bridging PNP Ligand Facilitates Ligand-to-Gold Electron Transfer.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017Article
- Pyridylidene ligand facilitates gold-catalyzed oxidative C-H arylation of heterocycles.Beilstein journal of organic chemistry · 2015Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Over the recent years, the nucleophilic manipulation of inactivated carbon-carbon double bonds has gained remarkable credit in the chemical community. As a matter of fact, despite lower reactivity with respect to alkynyl and allenyl counterparts, chemical functionalization of isolated alkenes, via carbon- as well as hetero atom-based nucleophiles, would provide direct access to theoretically unlimited added value of molecular motifs. In this context, homogenous [Au(I)] and [Au(III)] catalysis continues to inspire developments within organic synthesis, providing reliable responses to this interrogative, by combining crucial aspects such as chemical selectivity/efficiency with mild reaction parameters. This review intends to summarize the recent progresses in the field, with particular emphasis on mechanistic details.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.