HFIP-mediated C-3-alkylation of indoles and synthesis of indolo[2,3-<i>b</i>]quinolines & related natural products-Reference-Cited by-同舟云学术

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HFIP-mediated C-3-alkylation of indoles and synthesis of indolo[2,3-b]quinolines & related natural products

Published:2024 Issue:17 Volume:22 Page:3502-3509
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Rashid Auqib¹²³,Lone Waseem I.²³,Dogra Preeti²,Rashid Showkat²³^ORCID,Bhat Bilal A.¹³^ORCID

Affiliation:

1. Natural Products & Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Sanatnagar, Srinagar 190005, India

2. Natural Products & Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine Jammu, Jammu and Kashmir 180001, India

3. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India

Abstract

An expeditious metal free C-3 alkylation of indoles and its NIS-mediated deviation to indolo[2,3-b]quinolines is reported. Applications of these strategies in accessing bioactive natural products have also been demonstrated.

Funder

Science and Engineering Research Board

Council of Scientific and Industrial Research, India

Academy of Scientific and Innovative Research

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00414K

Reference97 articles.

1. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

3. Enantioselective Synthesis of Stephacidin B

4. Simple indole alkaloids and those with a non-rearranged monoterpenoid unit

5. Reserpine: A Challenge for Total Synthesis of Natural Products

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