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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c00425
Abstract: Herein, the first example using commercially available 2-bromo-3,3,3-trifluoropropene (BTP) as a radical acceptor has been reported. Taking advantage of this strategy, a wide range of secondary trifluoromethylated alkyl bromides were synthesized in good to excellent…
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Keywords:
bromo trifluoropropene;
alkyl bromides;
secondary trifluoromethylated;
trifluoromethylated alkyl ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c01390
Abstract: A nickel-catalyzed reductive cross-coupling reaction of aryl cyclopropyl ketones with easily accessible unactivated alkyl bromides to access aryl alkyl ketones has been developed. This strategy facilitates access to various of γ-alkyl-substituted ketones via ring opening…
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Keywords:
unactivated alkyl;
nickel catalyzed;
reductive coupling;
alkyl bromides ... See more keywords
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0
Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b01079
Abstract: A selective oxy-alkylation of allylamines with unactivated alkyl bromides and CO2 via visible-light-driven palladium catalysis is reported. The commercially available Pd(PPh3)4 is used as the sole catalyst in this three-component reaction. A variety of tertiary,…
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Keywords:
unactivated alkyl;
allylamines unactivated;
bromides co2;
alkylation allylamines ... See more keywords
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Published in 2019 at "Chemical Science"
DOI: 10.1039/c8sc04162h
Abstract: A migratory fluoro-alkenylation of unactivated alkyl bromides is reported; the reaction is enabled by fluorine effects and involves an alkyl nickel chain-walking mechanism.
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Keywords:
unactivated alkyl;
alkenylation unactivated;
alkyl bromides;
fluoro alkenylation ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c9cc04432a
Abstract: We here report the photoinduced Cu-catalyzed cyanoalkylation of electron-deficient alkenes by using alkyl bromides as alkylation reagents. In the reactions, 1°, 2°, and 3° unactivated alkyl bromides with various sensitive functional groups were well tolerated…
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Keywords:
unactivated alkyl;
alkyl bromides;
cyanoalkylation electron;
deficient alkenes ... See more keywords
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Published in 2020 at "Green Chemistry"
DOI: 10.1039/d0gc02855j
Abstract: Herein we report the first example of an on-water enantiospecific synthesis of alkyl bromides. This procedure allowed the conversion of secondary activated alkyl sulphides to benzylic alkyl bromides, which were obtained in high yields and…
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Keywords:
water;
alkyl bromides;
bromination mild;
enantiospecific water ... See more keywords
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1
Published in 2022 at "Chemical communications"
DOI: 10.1039/d2cc04210j
Abstract: A novel thio-Ritter-type reaction of alkyl bromides, nitriles, and hydrogen sulfide has been explored, providing a straightforward approach toward functionally important thioamides. This transformation features a broad substrate scope, operational simplicity, use of available feedstock…
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Keywords:
type reaction;
reaction;
alkyl bromides;
thio ritter ... See more keywords
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2
Published in 2023 at "Organic Chemistry Frontiers"
DOI: 10.1039/d3qo00096f
Abstract: A novel and efficient copper-catalyzed carboesterification of unactivated alkenes with α-carbonyl alkyl bromides for the syn-thesis of γ-lactones derivatives has been developed. With the assistance of a removable bidentate 8-aminoquinoline...
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Keywords:
carboesterification unactivated;
alkyl bromides;
carbonyl alkyl;
copper catalyzed ... See more keywords