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1
Published in 2020 at "ChemCatChem"
DOI: 10.1002/cctc.202001175
Abstract: Nucleophilic substitutions (SN) are typically promoted by acid chlorides as sacrificial reagents to improve the thermodynamic driving force and lower kinetic barriers. However, the cheapest acid chloride phosgene (COCl2) is a highly toxic gas. Against…
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Keywords:
catalysis enables;
enables activation;
base catalysis;
lewis base ... See more keywords
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1
Published in 2022 at "Organic Letters"
DOI: 10.1021/acs.orglett.2c00355
Abstract: Oxetanes are valuable building blocks due to their well-explored propensity to undergo ring-opening reactions with nucleophiles. However, their application as precursors of radical species is still elusive. Herein, we present a bioinspired cobalt-catalysis-based strategy to…
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Keywords:
catalysis enables;
cobalt catalysis;
nucleophilic radicals;
bioinspired cobalt ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b00884
Abstract: The synthesis and utilization of a class of 2,1-borazaronaphthyltrifluoroborate reagents that provide a general solution to the challenge of N-functionalization of the 2,1-borazaronaphthalene core is described. By adorning the nitrogen of this core with a…
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Keywords:
functionalized borazaronaphthalenes;
enables access;
photoredox catalysis;
access functionalized ... See more keywords
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1
Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c10785
Abstract: Design of ligands in transition-metal catalyzed reactions is challenging, especially in asymmetric transformations. With each step in the catalytic cycle promoted by its privileged ligand and different steps well-connected by dynamic ligand exchange, synergistic combination…
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Keywords:
enables asymmetric;
catalysis enables;
alkyl halides;
acylation ... See more keywords