PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 24, 2014Angewandte Chemie International Edition509 citationsOpen Access

Cobalt‐Catalyzed, Aminoquinoline‐Directed C(sp2)H Bond Alkenylation by Alkynes

View Full Paper
LGLiene GrigorjevaODOlafs Daugulis

Key Points

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

Abstract

A method for cobalt-catalyzed, aminoquinoline- and picolinamide-directed C(sp(2))-H bond alkenylation by alkynes was developed. The method shows excellent functional-group tolerance and both internal and terminal alkynes are competent substrates for the coupling. The reaction employs a Co(OAc)2⋅4 H2O catalyst, Mn(OAc)2 co-catalyst, and oxygen (from air) as a terminal oxidant.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Grigorjeva et al. (2014) studied this question.

synapsesocial.com/papers/6a62635fb3ffb27a727dd8eehttps://doi.org/10.1002/anie.201404579
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

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

  1. 1Rhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C−H Bond Cleavage2007 · 559 citations
  2. 2Copper-Catalyzed Etherification of Arene C–H Bonds2013 · 203 citations
  3. 3Nickel-Catalyzed Direct Arylation of C(sp3)–H Bonds in Aliphatic Amides via Bidentate-Chelation Assistance2013 · 407 citations
  4. 4Copper‐Mediated CH/CH Biaryl Coupling of Benzoic Acid Derivatives and 1,3‐Azoles2013 · 83 citations
  5. 5Pyrroloindolone Synthesis via a Cp*CoIII-Catalyzed Redox-Neutral Directed C–H Alkenylation/Annulation Sequence2014 · 463 citations