Solvent-controlled retention or inversion of configuration in the Suzuki reaction of 2-bromo-1,3-dienes: Stereodivergent synthesis of trisubstituted conjugated alkenes-Reference-Cited by-同舟云学术

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Solvent-controlled retention or inversion of configuration in the Suzuki reaction of 2-bromo-1,3-dienes: Stereodivergent synthesis of trisubstituted conjugated alkenes

Published:2022-11 Issue: Volume:126 Page:133011
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Shakhmaev Rinat N.^ORCID,Ignatishina Maria G.,Zorin Vladimir V.

Publisher

Elsevier BV

Reference63 articles.

1. (For representative reviews, see):

2. Handbook of Organopalladium Chemistry for Organic Synthesis;Negishi,2002

3. Ligand Effects on the Stereochemical Outcome of Suzuki–Miyaura Couplings

4. Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides

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2. Halogenation of aromatic compounds with N-halosuccinimides (NXS) catalysed by d-camphorsulfonic acid-BiCl₃;Organic & Biomolecular Chemistry;2024

3. Large acceleration of solvent-free Suzuki-Miyaura cross-coupling reactions at room temperature by the addition of small amounts of dioxane and water;Tetrahedron;2023-06

4. Solvent-controlled diastereodivergent cascade synthesis of trisubstituted tetrahydrothiophenes utilizing polystyrene-supported amine;Arkivoc;2023-04-25

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