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1
Published in 2018 at "ChemCatChem"
DOI: 10.1002/cctc.201801097
Abstract: Although allylation using allylic alcohol is an environmentally‐friendly method because of water being the sole byproduct in such reactions, allylic alcohol is one of the most difficult allylating agents in Pd‐catalyzed allylation of nucleophiles. In…
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Keywords:
catalyzed allylation;
allylic alcohols;
using allylic;
allylation using ... See more keywords
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0
Published in 2020 at "ChemCatChem"
DOI: 10.1002/cctc.202000442
Abstract: The asymmetric isomerization of primary allylic alcohols to chiral aldehydes using iridium‐catalysts bearing P,N‐MaxPHOX ligands has been studied. These catalysts can be fine‐tuned as they present three different stereogenic centers to modulate both the reactivity…
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Keywords:
primary allylic;
asymmetric isomerization;
maxphox ligands;
allylic alcohols ... See more keywords
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0
Published in 2021 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2021.153002
Abstract: Abstract A facile difluoroalkylation and 1,2-aryl migration reaction commencing from allylic alcohols and simple BrCF2COOEt was developed. This metal-free method offers chemists green and efficient access to important difluoro 1,5-dicarbonyl compounds in moderate to good…
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Keywords:
metal free;
aryl migration;
difluoroalkylation aryl;
allylic alcohols ... See more keywords
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0
Published in 2018 at "Chinese Journal of Catalysis"
DOI: 10.1016/s1872-2067(18)63028-1
Abstract: Abstract A novel nitrogen-centered radical-induced 1,2-carbon migration reaction of allylic alcohols has been developed. This method provides easy access to a variety of α-quaternary-β-amino ketones under mild reaction conditions. The reaction has a wide substrate…
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Keywords:
amino ketones;
quaternary amino;
carbon;
allylic alcohols ... See more keywords
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3
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04206
Abstract: A highly regioselective and catalyst-free sulfonation of allylic alcohols with sulfinyl amides has been realized. Such a mix-and-go procedure provides a convenient approach to synthetically various allylic sulfones under mild reaction conditions. Furthermore, this novel…
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Keywords:
allylic alcohols;
sulfinyl amides;
sulfonation;
sulfonation allylic ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03410
Abstract: The isomerization of allylic alcohols to the corresponding carbonyl compounds is a well-established reaction in organic synthesis. However, 1,3-carbon migration is a quite challenging field, and thus transformation has remained elusive until now. Herein, we…
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Keywords:
ruthenium catalyzed;
isomerization;
aryl redox;
allylic alcohols ... See more keywords
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.2c04243
Abstract: A novel strategy is demonstrated for Lewis base-activated trifluoromethylsulfinylation of allylic alcohols. Controllable synthesis of structurally varied allylic trifluoromethanesulfones via sigmatropic rearrangements was performed, and trifluoromethanesulfinate esters were achieved. This metal-free, catalytic divergent transformation features…
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Keywords:
allylic alcohols;
lewis base;
trifluoromethylsulfinylation allylic;
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00323
Abstract: A nickel-catalyzed direct reaction of allylic alcohols with benzyl nitrile derivatives has been developed. The method provides an efficient route for the synthesis of nitriles bearing an α-tertiary or quaternary carbon center in good to…
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Keywords:
direct substitution;
nickel catalyzed;
allylic alcohols;
catalyzed direct ... See more keywords
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00556
Abstract: A simple, efficient method has been developed for the CoIII-H-catalyzed aerobic C-C bond cleavage of tertiary allylic alcohols to access ketones. This novel approach presents excellent chemoselectivity, good functional group compatibility, and high yields. This…
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Keywords:
cleavage allylic;
allylic alcohols;
aerobic bond;
bond cleavage ... See more keywords
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0
Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b03627
Abstract: Carreira's iridium-(P, olefin) phosphoramidite-based catalytic system that allows asymmetric allyl-allylboronate cross-coupling with high enantioselectivity is reported. This transformation tolerates a large variety of racemic branched allylic alcohols and allylboronate substrates. The utility of the coupling…
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Keywords:
iridium catalyzed;
allyl;
allylic alcohols;
catalyzed enantioselective ... See more keywords
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0
Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b00735
Abstract: In this protocol, we report a Mo-catalyzed anti-dihydroxylation of secondary allylic alcohols, providing a general method for the preparation of 1,2,3-triols bearing up to three continuous stereocenters with excellent diastereocontrol. The mechanistic studies reveal that…
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Keywords:
dihydroxylation secondary;
dihydroxylation;
allylic alcohols;
molybdenum catalyzed ... See more keywords