Fischer indole synthesis applied to the total synthesis of natural products-Reference-Cited by-同舟云学术

Fischer indole synthesis applied to the total synthesis of natural products

Published:2017 Issue:83 Volume:7 Page:52852-52887
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Heravi Majid M.¹²³⁴⁵^ORCID,Rohani Sahar¹²³⁴⁵,Zadsirjan Vahideh¹²³⁴⁵,Zahedi Nazli¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. School of Science

3. Alzahra University

4. Tehran

5. Iran

Abstract

In this review, we are trying to underscore the application of FIS in one of the crucial step of indole construction in the total synthesis of biologically active natural products.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA10716A

Reference162 articles.

1. Total synthesis of new indolo[2,3-a]quinolizine alkaloids sempervirine type, potential pharmaceuticals

2. Indole Synthesis via Rhodium Catalyzed Oxidative Coupling of Acetanilides and Internal Alkynes

3. Formation of Enehydrazine Intermediates through Coupling of Phenylhydrazines with Vinyl Halides: Entry into the Fischer Indole Synthesis

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

5. Biomedical Importance of Indoles

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