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Published in 2019 at "ACS catalysis"
DOI: 10.1021/acscatal.9b04453
Abstract: Enantioselective conjunctive cross-coupling with propargylic carbonates affords (β-boryl allenes as the reaction product. The reaction is found to proceed through the intermediacy of dimethoxyboronate complexes that are generated in situ by a strain-induced ligand exchange…
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Keywords:
conjunctive cross;
catalytic enantioselective;
propargylic carbonates;
coupling propargylic ... See more keywords
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Published in 2018 at "Chemical communications"
DOI: 10.1039/c8cc04186e
Abstract: A highly efficient catalytic system consisting of Pd2(dba)3·CHCl3 and tri(o-tolyl)phosphine has been identified for the coupling of propargylic carbonates with different types of organo boronic acids at room temperature. Excellent central-to-axial chirality transfer was also…
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Keywords:
boronic acids;
propargylic carbonates;
coupling propargylic;
tri tolyl ... See more keywords
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Published in 2019 at "Chemical Science"
DOI: 10.1039/c9sc01703h
Abstract: Herein we describe an unprecedented RuII-catalyzed site-selective and regiospecific annulation of benzoic acids with propargylic carbonates. The weakly coordinating carboxylic acid moiety outperformed other typically used directing groups in C–H activation, including ketone, nitrile, sulfonamide,…
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Keywords:
site selective;
regiospecific annulation;
esi;
propargylic carbonates ... See more keywords
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Published in 2020 at "Chemical communications"
DOI: 10.1039/d0cc04986g
Abstract: Herein, a highly regioselective propargylic benzylation with propargylic carbonates and benzyl 1,4-dihydropyridine derivatives was developed via a photoredox/palladium dual-catalyzed process, which represents a novel catalytic model for non-terminal propargylic functionalization. The reaction showed excellent regioselectivity…
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Keywords:
propargylic benzylation;
photoredox palladium;
propargylic carbonates;