(Q45025739)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

A short total synthesis of the marine sponge pyrrole-2-aminoimidazole alkaloid (±)-agelastatin A (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Petar A Duspara

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

language of work or name

English

0 references

publication date

22 August 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

Angewandte Chemie International Edition

21 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

volume

52

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

issue

41

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

page(s)

10862-10866

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

Some recent advances in the synthesis of polycyclic imidazole-containing marine natural products

21 February 2020

cites work

1 reference

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Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids

21 January 2018

1 reference

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Agelastatins C and D, new pentacyclic bromopyrroles from the sponge Cymbastela sp., and potent arthropod toxicity of (-)-agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Agelastatin E, agelastatin F, and benzosceptrin C from the marine sponge Agelas dendromorpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Inhibition of cyclin-dependent kinases, GSK-3beta and CK1 by hymenialdisine, a marine sponge constituent

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Selective small-molecule inhibitors of glycogen synthase kinase-3 activity protect primary neurones from death

21 January 2018

1 reference

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Full reversal of Alzheimer's disease-like phenotype in a mouse model with conditional overexpression of glycogen synthase kinase-3.

21 January 2018

1 reference

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AR-A014418, a selective GSK-3 inhibitor, produces antidepressant-like effects in the forced swim test

21 January 2018

1 reference

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Agelastatin A: a novel inhibitor of osteopontin-mediated adhesion, invasion, and colony formation

21 January 2018

1 reference

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Alkynyliodonium salts in organic synthesis. Application to the total synthesis of (-)-agelastatin A and (-)-agelastatin B.

21 January 2018

1 reference

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New class of nucleophiles for palladium-catalyzed asymmetric allylic alkylation. Total synthesis of agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Total synthesis of (+/-)-agelastatin A, a potent inhibitor of osteopontin-mediated neoplastic transformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

A stereoselective synthesis of the bromopyrrole natural product (-)-agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Total synthesis of all (-)-Agelastatin alkaloids

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Bioinspired total synthesis of agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Enantiospecific formal total synthesis of the tumor and GSK-3 beta inhibiting alkaloid, (-)-agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Stereocontrolled synthesis of vicinal diamines by organocatalytic asymmetric Mannich reaction of N-protected aminoacetaldehydes: formal synthesis of (-)-agelastatin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Formal synthesis of (-)-agelastatin A: an iron(II)-mediated cyclization strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Alkynyliodonium salts in organic synthesis. Development of a unified strategy for the syntheses of (-)-agelastatin A and (-)-agelastatin B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: agelastatin A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Practical enantiospecific synthesis of an orthogonally protected 1,4-trans-1,5-cis- 4,5-diamino-2-cyclopenten-1-ol derivative

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Aiming for the ideal synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Design Constraints in Practical Syntheses of Complex Molecules: Current Status, Case Studies with Carbohydrates and Alkaloids, and Future Perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Total synthesis of marine natural products without using protecting groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Protecting-group-free synthesis as an opportunity for invention

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Green chemistry for chemical synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Chemoselectivity: the mother of invention in total synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

The atom economy--a search for synthetic efficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Function-oriented synthesis, step economy, and drug design

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Redox economy in organic synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Enantioselective total syntheses of manzamine a and related alkaloids

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Amide bond formation and peptide coupling

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Amide bond formation: beyond the myth of coupling reagents

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Peptide coupling reagents, more than a letter soup

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Rethinking amide bond synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

Search for optimal coupling reagent in multiple peptide synthesizer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201304759

The Active Centres of Agelastatin A, a Strongly Cytotoxic Alkaloid of the Coral Sea Axinellid SpongeAgelas dendromorpha, as Determined by Comparative Bioassays with Semisynthetic Derivatives

21 January 2018

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.19960790315

Identifiers

DOI

10.1002/ANIE.201304759

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24038621%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference