Mizoroki–Heck reaction of 1,2-disubstituted aryl alkenes: Variables of synthesis, solvent and ligand modulation of reactivity
Author:
Affiliation:
1. Organic Chemistry Division, National Chemical Laboratory, Pune, Maharashtra, India
2. Academy of Scientific and Innovative Research (AcSIR), New Delhi, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2020.1811986
Reference52 articles.
1. The Mizoroki–Heck Reaction
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3. Palladium-Catalyzed Olefinations of Aryl Halides (Heck Reaction) and Related Transformations
4. Beletskaya, I. P.; Cheprakov, A. V. RSC Catalysis Series, (Trends in Cross –Couplings), London, UK, 2015; Vol. 21, pp 355–478.
5. Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide
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1. Double Mirozoki-Heck arylation of terminal alkenes using “ligand-free” pd catalytic systems;Журнал органической химии;2023-12-15
2. Double Mizoroki–Heck Arylation of Terminal Alkenes in the Presence of “Ligand-Free” Palladium Catalytic Systems;Russian Journal of Organic Chemistry;2023-10
3. The local and natural sources in synthetic methods: the practical synthesis of aryl oximes from aryl aldehydes under catalyst-free conditions in mineral water;Journal of Chemical Sciences;2021-07-20
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