(Q42934197)

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A concise silylamine approach to 2-amino-3-hydroxy-indoles with potent in vivo antimalaria activity

scientific article published on September 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

11 November 2017

A concise silylamine approach to 2-amino-3-hydroxy-indoles with potent in vivo antimalaria activity (English)

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Europe PubMed Central

PubMed publication ID

11 November 2017

6

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Dyann F Wirth

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Europe PubMed Central

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11 November 2017

Ralph Mazitschek

8

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Ralph Mazitschek

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7

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Jon Clardy

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Europe PubMed Central

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11 November 2017

author name string

Sameer Urgaonkar

1

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Europe PubMed Central

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11 November 2017

Joseph F Cortese

2

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Europe PubMed Central

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11 November 2017

Robert H Barker

3

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11 November 2017

Mandy Cromwell

4

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11 November 2017

Adelfa E Serrano

5

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11 November 2017

Ralph Mazitschek

8

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11 November 2017

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publication date

1 September 2010

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11 November 2017

Organic Letters

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11 November 2017

12

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11 November 2017

18

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Europe PubMed Central

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11 November 2017

3998-4001

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PubMed publication ID

11 November 2017

Catalytic asymmetric synthesis of substituted 3-hydroxy-2-oxindoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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New ammonia equivalents for the Pd-catalyzed amination of aryl halides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

based on heuristic

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Rhodium-catalyzed asymmetric addition of aryl- and alkenylboronic acids to isatins

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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One-step RhCl3-catalyzed deprotection of acyclic N-allyl amides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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Rhodium-catalyzed addition of arylboronic acids to isatins: an entry to diversity in 3-aryl-3-hydroxyoxindoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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Chemical genetics of Plasmodium falciparum

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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Synthesis and structure-activity relationships of 3-aryloxindoles: a new class of calcium-dependent, large conductance potassium (maxi-K) channel openers with neuroprotective properties

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

based on heuristic

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In vitro evaluations of antimalarial drugs and their relevance to clinical outcomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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Thousands of chemical starting points for antimalarial lead identification

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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High-throughput Plasmodium falciparum growth assay for malaria drug discovery

1 reference

https://pubmed.ncbi.nlm.nih.gov/20718474

12 December 2020

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Identifiers

10.1021/OL101566H

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

PMC publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

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