Synthesis of Azepinoindoles and Oxepinoindoles through Brønsted-Acid-Catalyzed Cyclization of an <i>In Situ</i> Generated Dihydrospiroquinoline Intermediate-Reference-Cited by-同舟云学术

Synthesis of Azepinoindoles and Oxepinoindoles through Brønsted-Acid-Catalyzed Cyclization of an In Situ Generated Dihydrospiroquinoline Intermediate

Published:2024-05-01 Issue:18 Volume:26 Page:3911-3916
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mahato Rina¹,Yadav Naveen¹,Hazra Chinmoy Kumar¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India

Funder

Council of Scientific and Industrial Research, India

University Grants Commission

Science and Engineering Research Board

Ministry of Education, India

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01091

Reference27 articles.

1. Synthesis of Azepino[4,5-b]indole via Ring Expansion of Tetrahydro-β-carbolines Ammonium Ylide

2. Arboflorine, an Unusual Pentacyclic Monoterpenoid Indole Alkaloid Incorporating a Third Nitrogen Atom

3. Indole-fused azepines and analogues as anticancer lead molecules: Privileged findings and future directions

4. Stereocomplementary Chemoenzymatic Pictet–Spengler Reactions for Formation of Rare Azepino-indole Frameworks: Discovery of Antimalarial Compounds

5. Repurposing cancer drugs identifies kenpaullone which ameliorates pathologic pain in preclinical models via normalization of inhibitory neurotransmission

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