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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c00499
Abstract: Herein, we report the first diaryliodonium salts promoted multicomponent 1,2,3-trifunctionalization of alkynes, where both the acetylenic bond and the adjacent nonactivated propargylic C(sp3)-H bond were functionalized synergistically to generate α-arylated enones with high chemo-, regio-,…
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Keywords:
multicomponent trifunctionalization;
chemo regio;
internal alkynes;
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b00099
Abstract: Described herein is a palladium-catalyzed dearomative annulation of alkyl bromoarenes with internal alkynes. Challenges in this spiroannulation include the chemoselectivity among [2 + 2 + 1], [2 + 2 + 2], and [3 + 2]…
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Keywords:
heck type;
internal alkynes;
alkyl bromoarenes;
bromoarenes internal ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c9cc03391b
Abstract: The first chemo-, regio-, and enantioselective rhodium-catalyzed addition of oximes to allenes is reported. Using a Rh(i)/Josiphos catalyst system under mild conditions, the construction of allylic C-N bonds instead of C-O bonds was achieved. This…
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Keywords:
catalyzed addition;
regio enantioselective;
rhodium catalyzed;
oximes allenes ... See more keywords
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Published in 2022 at "Chemical Science"
DOI: 10.1039/d2sc00294a
Abstract: The 1,1,2,2-tetrafluoroethylene unit is prevalent in bioactive molecules and functional materials. Despite being in principle a straightforward strategy to access this motif, the direct tetrafluorination of alkynes involves very hazardous or inconvenient reagents. Therefore, safer…
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Keywords:
fluorinated alkyl;
chemo regio;
regio divergent;
alkynyl triazenes ... See more keywords