(Q35160884)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24786845%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

title

Non-conventional methodologies in the synthesis of 1-indanones (English)

1 reference

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17 March 2020

6

1 reference

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17 March 2020

author name string

Manuela Oliverio

1

1 reference

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17 March 2020

Monica Nardi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24786845%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Paola Costanzo

3

1 reference

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17 March 2020

Luca Cariati

4

1 reference

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17 March 2020

Giancarlo Cravotto

5

1 reference

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17 March 2020

Antonio Procopio

7

1 reference

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17 March 2020

language of work or name

English

0 references

publication date

30 April 2014

1 reference

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17 March 2020

1 reference

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17 March 2020

volume

19

1 reference

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17 March 2020

issue

5

1 reference

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17 March 2020

page(s)

5599-5610

1 reference

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Creative Commons Attribution 4.0 International

17 March 2020

copyright license

start time

30 April 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis.

1 reference

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The concise synthesis of chalcone, indanone and indenone analogues of combretastatin A4.

21 January 2018

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Gallic acid-based indanone derivatives as anticancer agents.

21 January 2018

1 reference

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Indanocine, a microtubule-binding indanone and a selective inducer of apoptosis in multidrug-resistant cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Dilemmaones A-C, unusual indole alkaloids from a mixed collection of south african sponges

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Recent developments in the Nazarov process

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Conversion of indanone oximes into isocarbostyrils

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Palladium-Catalyzed Carbonylative Cyclization of Unsaturated Aryl Iodides and Dienyl Triflates, Iodides, and Bromides to Indanones and 2-Cyclopentenones

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Polyphosphoric Acids As A Reagent In Organic Chemistry

21 January 2018

1 reference

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Controlled microwave heating in modern organic synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FMOLECULES19055599

Phosphorus pentoxide-methanesulfonic acid. Convenient alternative to polyphosphoric acid

21 January 2018

1 reference

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Convenient access to polysubstituted 1-indanones by Sc(OTf)3-catalyzed intramolecular Friedel-Crafts acylation of benzyl Meldrum's acid derivatives

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24786845

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Synthesis and pharmacological evaluation of the individual stereoisomers of 3-[methyl(1,2,3,4-tetrahydro-2-naphthalenyl)amino]-1-indanone, a potent mast cell stabilising agent

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24786845

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3390/MOLECULES19055599

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24786845%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24786845%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

PubMed publication ID

24786845

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24786845%20AND%20SRC:MED&resulttype=core&format=json