4.8 Article

Directing Group Enhanced Carbonylative Ring Expansions of Amino-Substituted Cyclopropanes: Rhodium-Catalyzed Multicomponent Synthesis of N-Heterobicyclic Enones

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 13, Pages 4992-4995

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja401936c

Keywords

-

Funding

  1. EPSRC [EP/G036764/1]
  2. Syngenta
  3. Royal Society
  4. EPSRC [EP/K03927X/1] Funding Source: UKRI
  5. Engineering and Physical Sciences Research Council [981180, EP/K03927X/1] Funding Source: researchfish

Ask authors/readers for more resources

Aminocyclopropanes equipped with suitable N-directing groups undergo efficient and regioselective Rh-catalyzed carbonylative C-C bond activation. Trapping of the resultant metallacycles with tethered alkynes provides an atom-economic entry to diverse N-heterobicyclic enones. These studies provide a blueprint for myriad N-heterocyclic methodologies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available