2005
DOI: 10.1039/b316241a
|View full text |Cite
|
Sign up to set email alerts
|

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

Abstract: This review covers newly isolated simple indole alkaloids, structure determinations, total syntheses and biological activities reported in the literature in 2003.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
103
0
2

Year Published

2006
2006
2018
2018

Publication Types

Select...
5
4
1

Relationship

0
10

Authors

Journals

citations
Cited by 519 publications
(106 citation statements)
references
References 194 publications
0
103
0
2
Order By: Relevance
“…Indole scaffolds have been known for their value in the development of new compounds of pharmaceutical interest. [18][19][20] Up to date, several 21,22 Herein, in continuation of our studies towards the synthesis of heterocyclic compounds and multicomponent reactions, [23][24][25][26][27][28][29][30][31][32] and since there is a wide range of reactions that include indole in the preparation of heterocyclic compounds, this review presents the recent applications of indole in the synthesis of diverse heterocyclic compounds during the period from 2012 to 2017. This review rst discusses indoles' C-3 carbon atom reactivity applicable to electrophilic reactions, followed by MCRs in which the N position of indole is reacted as a nucleophile to afford N-substituted indole products.…”
Section: Introductionmentioning
confidence: 99%
“…Indole scaffolds have been known for their value in the development of new compounds of pharmaceutical interest. [18][19][20] Up to date, several 21,22 Herein, in continuation of our studies towards the synthesis of heterocyclic compounds and multicomponent reactions, [23][24][25][26][27][28][29][30][31][32] and since there is a wide range of reactions that include indole in the preparation of heterocyclic compounds, this review presents the recent applications of indole in the synthesis of diverse heterocyclic compounds during the period from 2012 to 2017. This review rst discusses indoles' C-3 carbon atom reactivity applicable to electrophilic reactions, followed by MCRs in which the N position of indole is reacted as a nucleophile to afford N-substituted indole products.…”
Section: Introductionmentioning
confidence: 99%
“…Because of the large number of biologically interesting natural products bearing highly functionalized indole skeletons [47][48][49], Fischer indole synthesis has received considerable synthetic interest. As a consequence, microwave-assisted Fischer indole synthesis has recently been investigated as a key step in the synthesis of a large number of indole alkaloids and their structural analogues.…”
Section: Synthesis Of Alkaloidsmentioning
confidence: 99%
“…[12] An obvious extension of the described SmI 2 -induced cyclization-dearomatization reaction involved the employment of N-heteroaromatic ring systems, such as quinoline, [13] pyrrole, and indole derivatives. [14] The general importance of N-heterocycles, of indole derivatives in particular, [15] originates from their ubiquitous presence in natural products and pharmaceutically relevant compounds. Among these, strychnos alkaloids belong to the most fascinating indole derivatives.…”
Section: Introductionmentioning
confidence: 99%