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

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21 February 2020

2

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21 February 2020

author name string

Petar A Duspara

series ordinal

1

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21 February 2020

language of work or name

English

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publication date

22 August 2013

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Angewandte Chemie International Edition

21 February 2020

published in

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volume

52

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issue

41

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page(s)

10862-10866

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

21 February 2020

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

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

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

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

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

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

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

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

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

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

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

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Total synthesis of all (-)-Agelastatin alkaloids

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Bioinspired total synthesis of agelastatin A.

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis1

21 January 2018

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Search for optimal coupling reagent in multiple peptide synthesizer

21 January 2018

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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

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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

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