Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
March 2, 2009Organic Letters

Direct Amination of Azoles via Catalytic C−H, N−H Coupling

View Full Paper
Ask AI
Bookmark
Share

Authors

DMDaiki MonguchiKyoto UniversityTFTaiki FujiwaraKobe UniversityHFHirotoshi FurukawaKanazawa University

Discussion

Loading...

Member takes

Implication

Key Points

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

Cite This Study

Monguchi et al. (2009) studied this question.

synapsesocial.com/papers/6a75d69173aee6431613d09chttps://doi.org/10.1021/ol900298e
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. 1Activated Aryl Chlorides: Useful Partners for the Coupling with 2‐Substituted Thiazoles in the Palladium‐Catalysed C‐H Activation/Functionalisation Reaction2007 · 68 citations
  2. 2Intermolecular Amidation of Unactivated sp<sup>2</sup> and sp<sup>3</sup> C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion2006 · 672 citations
  3. 3Toward a Synthetically Useful Stereoselective C−H Amination of Hydrocarbons2007 · 381 citations
  4. 4Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides1994 · 845 citations
  5. 5Synthesis of β-, γ-, and δ-Lactams via Pd(II)-Catalyzed C−H Activation Reactions2008 · 493 citations