Mechanism and reactivity of catalytic propargylic substitution reactions via metal–allenylidene intermediates: a theoretical perspective

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Mechanism and reactivity of catalytic propargylic substitution reactions via metal–allenylidene intermediates: a theoretical perspective

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im Januar 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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Mechanism and reactivity of ca ...... tes: a theoretical perspective

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P1476

Mechanism and reactivity of ca ...... tes: a theoretical perspective

@en

P2093

Ken Sakata

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P2860

Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group.

Palladium-catalysed formation of vicinal all-carbon quaternary centres via propargylation

Nickel-catalyzed Negishi cross-couplings of secondary nucleophiles with secondary propargylic electrophiles at room temperature.

Isolation of cationic and neutral (allenylidene)(carbene) and bis(allenylidene)gold complexes.

Allenylidene and higher cumulenylidene complexes.

HBF4-Catalysed Nucleophilic Substitutions of Propargylic Alcohols

Enantioselective propargylic [1,3]-rearrangements: copper-catalyzed O-to-N migrations toward C-N bond formation.

Propargylic activation across a heterobimetallic ir-sn catalyst: nucleophilic substitution and indene formation with propargylic alcohols.

Facile one-pot synthesis of three different substituted thiazoles from propargylic alcohols.

Ruthenium-triggered ring opening of ethynylcyclopropanes: [3+2] cycloaddition with aldehydes and aldimines involving metal allenylidene intermediates.

P304

12-25

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P31

scholarly article

P356

10.1039/C7CY01382E

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Yoshiaki Nishibayashi

P577

2018-01-01T00:00:00Z

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