Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
June 13, 2024SynthesisOpen Access

Latest Developments in Palladium and Nickel-Catalyzed Cross-Couplings for Aryl Chlorides: Suzuki-Miyaura and Buchwald-Hartwig Reactions

View Full Paper
Ask AI
Bookmark
Share

Authors

YYYoichi M. A. YamadaKyushu UniversityASAbhijit SenRIKEN Center for Sustainable Resource Science

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Yamada et al. (2024) studied this question.

synapsesocial.com/papers/68e64d72b6db6435875de408https://doi.org/10.1055/a-2344-5677
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Suzuki‐Miyaura and Buchwald‐Hartwig Cross‐Coupling Reactions Utilizing a Set of Complementary Imidazopyridine Monophosphine Ligands2024 · 1 citations
  2. 2Transition-Metal-Catalyzed Direct Arylation of Ammonia2024 · 3 citations
  3. 3A highly efficient and recyclable NiCl <sub>2</sub> (dppp)/PEG-400 system for Suzuki-Miyaura reaction of aryl chlorides with arylboronic acids2019 · 10 citations
  4. 4Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides2020 · 11 citations
  5. 5Design and synthesis of a new phosphinite-functionalized clay composite for the stabilization of palladium nanoparticles. Application as a recoverable catalyst for C–C bond formation reactions2014 · 28 citations