Structurally diverse hamigerans from the New Zealand marine sponge Hamigera tarangaensis: NMR-directed isolation, structure elucidation and antifungal activity. (Q39113706)

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scientific article published on December 2013

Language	Label	Description	Also known as
English	Structurally diverse hamigerans from the New Zealand marine sponge Hamigera tarangaensis: NMR-directed isolation, structure elucidation and antifungal activity.	scientific article published on December 2013

Statements

scholarly article

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7 March 2020

Structurally diverse hamigerans from the New Zealand marine sponge Hamigera tarangaensis: NMR-directed isolation, structure elucidation and antifungal activity (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23925673%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

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Hamigera tarangaensis

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Hamigeran A ethyl ester

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Ethyl 7-bromo-4,6-dihydroxy-3a,8-dimethyl-5-oxo-1-propan-2-yl-1,2,3,9b-tetrahydrocyclopenta[a]naphthalene-4-carboxylate

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3-Bromo-6-[2-(carboxymethyl)-2-methyl-5-propan-2-ylcyclopentyl]-2-hydroxy-4-methylbenzoic acid

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Methyl 7-bromo-5,6-dihydroxy-3a,8-dimethyl-4-oxo-1-propan-2-yl-1,2,3,9b-tetrahydrocyclopenta[a]naphthalene-5-carboxylate

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1 reference

7-bromo-4,6-dihydroxy-3a,8-dimethyl-1-propan-2-yl-2,3,4,9b-tetrahydro-1H-cyclopenta[a]naphthalen-5-one

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(6,7-dihydroxy-3a,6,9-trimethyl-5-oxo-1-propan-2-yl-2,3,4,10b-tetrahydro-1H-benzo[e]azulen-4-yl) acetate

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Hamigeran L 11-O-methyl ester

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2-{7-bromo-6-hydroxy-1,4,4,8-tetramethyl-5-oxo-2H,3H,3aH,9bH-cyclopenta[a]naphthalen-1-yl}-2-oxoethyl acetate

1 reference

(6-Bromo-7,9-dihydroxy-5,12,15,15-tetramethyl-11-oxo-10-tetracyclo[7.5.1.02,12.03,8]pentadeca-3(8),4,6-trienyl) acetate

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4-bromohamigeran K

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8-bromo-7-hydroxy-3a,9-dimethyl-1-propan-2-yl-2,3,4,10b-tetrahydro-1H-benzo[e]azulene-5,6-dione

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3-Bromo-2-hydroxy-6-[2-(2-methoxy-2-oxoethyl)-2-methyl-5-propan-2-ylcyclopentyl]-4-methylbenzoic acid

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12-Acetoxy-13-epi-neoverrucosan-5-one

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7,9-dibromo-4,6-dihydroxy-3a,8-dimethyl-1-propan-2-yl-2,3,4,9b-tetrahydro-1H-cyclopenta[a]naphthalen-5-one

1 reference

A. Jonathan Singh

1

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7 March 2020

author name string

Jonathan D Dattelbaum

2

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7 March 2020

Jessica J Field

3

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7 March 2020

Zlatka Smart

4

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7 March 2020

Ethan F Woolly

5

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7 March 2020

Jacqueline M Barber

6

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7 March 2020

Rosemary Heathcott

7

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7 March 2020

John H Miller

8

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7 March 2020

Peter T Northcote

9

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7 March 2020

publication date

1 December 2013

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7 March 2020

Organic and Biomolecular Chemistry

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7 March 2020

11

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7 March 2020

46

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7 March 2020

8041-8051

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7 March 2020

Synthesis of (+/-)-hamigeran B, (-)-hamigeran B, and (+/-)-1-epi-hamigeran B: use of bulky silyl groups to protect a benzylic carbon-oxygen bond from hydrogenolysis

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Total synthesis of hamigerans and analogues thereof. Photochemical generation and Diels-Alder trapping of hydroxy-o-quinodimethanes

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

An asymmetric synthesis of hamigeran B via a Pd asymmetric allylic alkylation for enantiodiscrimination

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Synthesis of (-)-hamigeran B.

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Biosynthesis via carbocations: theoretical studies on terpene formation.

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Mitochondrial genome-knockout cells demonstrate a dual mechanism of action for the electron transport complex I inhibitor mycothiazole.

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Exploring the Mode-of-Action of Bioactive Compounds by Chemical-Genetic Profiling in Yeast

1 reference

https://api.crossref.org/works/10.1039%2FC3OB41305E

21 January 2018

Stereospecific total synthesis of the antiviral agent hamigeran B--use of large silyl groups to enforce facial selectivity and to suppress hydrogenolysis

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/ANIE.200351519

Identifiers

10.1039/C3OB41305E

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Europe PubMed Central

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7 March 2020

release_34jupjkjarhrvg32fyfsitwrbi

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24 November 2022

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mapped directly with Wikidata item

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7 March 2020

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