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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04135
Abstract: Robust air-stable cyclometalated π-allyliridium C,O-benzoates modified by (S)-tol-BINAP catalyze the reaction of secondary aliphatic amines with racemic alkyl-substituted allylic acetates to furnish products of allylic amination with high levels of enantioselectivity. Complete branched regioselectivities were…
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Keywords:
amination;
regio enantioselective;
substituted allylic;
alkyl substituted ... See more keywords
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Published in 2022 at "ACS catalysis"
DOI: 10.1021/acscatal.2c01647
Abstract: Iridium-tol-BINAP-catalyzed reductive coupling of allylic acetates with oxetanones and azetidinones mediated by 2-propanol provides chiral α-stereogenic oxetanols and azetidinols. As illustrated in 50 examples, complex, nitrogen-rich substituents that incorporate the top 10 N-heterocycles found in…
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Keywords:
stereogenic oxetanols;
reductive coupling;
oxetanols azetidinols;
allylic acetates ... See more keywords
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Published in 2019 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.8b12152
Abstract: The air- and water-stable π-allyliridium C,O-benzoate modified by ( S)-tol-BINAP, ( S)-Ir-II, catalyzes highly regio- and enantioselective Tsuji-Trost-type aminations of racemic branched alkyl-substituted allylic acetates using primary or secondary (hetero)aromatic amines. Specifically, in the presence…
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Keywords:
branched alkyl;
regio enantioselective;
primary secondary;
amination ... See more keywords