Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
March 13, 2017Angewandte Chemie International Edition

Synthesis of C3‐Fluorinated Oxindoles through Reagent‐Free Cross‐Dehydrogenative Coupling

View Full Paper
Ask AI
Bookmark
Share

Authors

ZWZheng‐Jian WuHXHai‐Chao Xu

Discussion

Loading...

Member takes

Overview

Key Points

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

Cite This Study

Wu et al. (2017) studied this question.

synapsesocial.com/papers/6a6cdabdf44fa9f079db6a69https://doi.org/10.1002/anie.201701329
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1First C−H Activation Route to Oxindoles using Copper Catalysis2010 · 190 citations
  2. 2Catalytic Enantioselective Fluorination of Oxindoles2005 · 348 citations
  3. 3Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent‐ and Metal‐Free Anodic Cross‐Coupling Reaction2016 · 162 citations
  4. 4Cinchona Alkaloid Catalyzed Enantioselective Fluorination of Allyl Silanes, Silyl Enol Ethers, and Oxindoles2008 · 115 citations