Ruthenium(II)‐Catalyzed C−H/C−H (4+2) Annulation of 2‐Aryl‐N‐heterocycles with Vinylene Carbonate

A ruthenium(II)-catalyzed direct C-H/C-H (4+2) annulation of 2-aryl-N-heterocycles such as 2-aryl-4H-pyrido[1,2-a]pyrimidin-4-ones, 2-arylimidazo[1,2-a]pyridines, 2-aryl-2H-indazoles and 2-arylquinolin-4(1H)-ones with vinylene carbonate has been described. This one-pot cascade strategy provided the diversely substituted fused-polyheterocycles such as 7H-benzo[h]pyrido[2,1-b]quinazolin-7-ones, naphtho[1',2':4,5]imidazo[1,2-a]pyridines, indazolo[2,3-a]quinolines and benzo[c]acridin-7(12H)-ones in moderate to excellent yields. The developed protocol exhibited a broad substrate scope with good functional group tolerance and acid/base-free conditions. Based on a preliminary mechanistic investigation, a tentative mechanism of Ru(II)-catalyzed (4+2) annulation reaction has been proposed.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2024-11-24
DOI
https://doi.org/10.1002/asia.202401104
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
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article
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article

Ruthenium(II)‐Catalyzed C−H/C−H (4+2) Annulation of 2‐Aryl‐N‐heterocycles with Vinylene Carbonate

Krishnan Rangan, Dhananjay S. Nipate, Anil Kumar, Amol B. Gadekar et al.
1 citations
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
0.25
article

Ruthenium(II)‐Catalyzed C−H/C−H (4+2) Annulation of 2‐Aryl‐N‐heterocycles with Vinylene Carbonate

Krishnan Rangan, Dhananjay S. Nipate, Anil Kumar, Amol B. Gadekar, Prakash N. Swami, Tarun Jangir
article en
1 citations

Abstract

A ruthenium(II)-catalyzed direct C-H/C-H (4+2) annulation of 2-aryl-N-heterocycles such as 2-aryl-4H-pyrido[1,2-a]pyrimidin-4-ones, 2-arylimidazo[1,2-a]pyridines, 2-aryl-2H-indazoles and 2-arylquinolin-4(1H)-ones with vinylene carbonate has been described. This one-pot cascade strategy provided the diversely substituted fused-polyheterocycles such as 7H-benzo[h]pyrido[2,1-b]quinazolin-7-ones, naphtho[1',2':4,5]imidazo[1,2-a]pyridines, indazolo[2,3-a]quinolines and benzo[c]acridin-7(12H)-ones in moderate to excellent yields. The developed protocol exhibited a broad substrate scope with good functional group tolerance and acid/base-free conditions. Based on a preliminary mechanistic investigation, a tentative mechanism of Ru(II)-catalyzed (4+2) annulation reaction has been proposed.

Chemistry - An Asian JournalVol. 20(3)
Birla Institute of Technology and Science - Hyderabad Campus (IN), Birla Institute of Technology and Science, Pilani (IN)
Openalex Percentile: Top 46%
Catalytic C–H Functionalization Methods
0.25
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Ruthenium(II)‐Catalyzed C−H/C−H (4+2) Annulation of 2‐Aryl‐N‐heterocycles with Vinylene Carbonate — Krishnan Rangan, Dhananjay S. Nipate, et al. · Chemistry - An Asian Journal (2024) | TGRS Research Map | TGRS