Site-Selective Electrophilic Cyclization and Subsequent Ring-Opening: A Synthetic Route to Pyrrolo[1,2-a]quinolines and Indolizines-Reference-Cited by-同舟云学术

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Site-Selective Electrophilic Cyclization and Subsequent Ring-Opening: A Synthetic Route to Pyrrolo[1,2-a]quinolines and Indolizines

Published:2012-09-17 Issue:19 Volume:77 Page:8562-8573
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Aggarwal Trapti¹,Kumar Sonu¹,Dhaked Devendra K.²,Tiwari Rakesh K.¹³,Bharatam Prasad V.²,Verma Akhilesh K.¹

Affiliation:

1. Synthetic Organic Chemistry Research Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India

2. Department of Medicinal Chemistry, NIPER, Punjab Mohali, 160062 India

3. Department of Biomedical & Pharmaceutical Sciences, University of Rhode Island, Kingston, Rhode Island, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo3015374

Reference64 articles.

1. Silver Triflate-Catalyzed or Electrophile-Mediated Tandem Reaction ofN′-(2-Alkynylbenzylidene)hydrazides with Dimethyl Acetylenedicarboxylate

2. Domino Process in Silver-Catalyzed Reactions of N-Arylformimidates and Active Methylene Compounds Involving Cycloisomerization and 1,3-Alkenyl Shift

3. Gold- or Platinum-Catalyzed Tandem Cycloisomerization/Prins-Type Cyclization Reactions

4. Rhodium-Catalyzed Tandem Cyclization: Formation of 1H-Indenes and 1-Alkylideneindans from Arylboronate Esters in Aqueous Media

5. Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis

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1. Exploration of Synthetic Potential of Quinoline‐3‐Carbaldehydes;European Journal of Organic Chemistry;2024-09-05

2. Recent advances in the synthesis of pyrrolo[1,2-a]quinolines;Chemistry of Heterocyclic Compounds;2023-12

3. Pyrazole‐promoted synthesis of pyrrolo[3,4‐c] quinoline-1,3‐diones in a novel diketene-based reaction;Frontiers in Chemistry;2023-09-26

4. Divergent access to 5,6,7-perifused cycles;Nature Communications;2023-08-24

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