Antifungal Diterpene Alkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational Assignments of Agelasidines and Agelasines (Q37642787)

21 August 2017

Antifungal Diterpene Alkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational Assignments of Agelasidines and Agelasines (English)

1 reference

21 August 2017

1 reference

Agelas citrina

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E Paige Stout

1 reference

21 August 2017

Lily C Yu

series ordinal

1 reference

21 August 2017

Tadeusz F Molinski

series ordinal

1 reference

21 August 2017

1 September 2012

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European Journal of Organic Chemistry

21 August 2017

1 reference

21 August 2017

2012

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21 August 2017

1 reference

21 August 2017

5131-5135

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INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTS

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Pyrrole aminoimidazole alkaloid metabiosynthesis with marine sponges Agelas conifera and Stylissa caribica

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

De novo synthesis of benzosceptrin C and nagelamide H from 7-15N-oroidin: implications for pyrrole-aminoimidazole alkaloid biosynthesis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Antimicrobial metabolites from the Paracel Islands sponge Agelas mauritiana

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Pinene cyclases I and II. Two enzymes from sage (Salvia officinalis) which catalyze stereospecific cyclizations of geranyl pyrophosphate to monoterpene olefins of opposite configuration.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Short, enantioselective total synthesis of sceptrin and ageliferin by programmed oxaquadricyclane fragmentation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Atomic contributions to the optical rotation angle as a quantitative probe of molecular chirality

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Synthetic and model computational studies of molar rotation additivity for interacting chiral centers: A reinvestigation of van't Hoff's principle

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3957321

Agelasine-A, -B, -C and -D, novel bicyclic diterpenoids with a 9-methyladeninium unit possessing inhibitory effects on na,K-atpase from the okinawa sea sponge sp.1)

1 September 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.201200572

Agelasines J, K, and L from the Solomon Islands Marine Sponge Agelas cf. mauritiana

21 January 2018

1 reference

12 December 2020

Agelasine G, a new antileukemic alkaloid from the Okinawan marine sponge Agelas sp

1 reference

12 December 2020

Agelasines H and I, 9-methyladenine-containing diterpenoids from an Agelas sponge

1 reference

12 December 2020

(-)-agelasidine C and (-)-agelasidine D, two new hypotaurocyamine diterpenoids from the Caribbean sea sponge Agelas clathrodes

1 reference

12 December 2020

Physiologically active marine natural products from Porifera. VIII. Agelasidines. Novel hypotaurocyamine derivatives from the Okinawan sea sponge Agelas nakamurai Hoshino

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.201200572

7 January 2021

inferred from DOI database lookup

Configurational analysis of new furanosesquiterpenes from Dysidea herbacea. Assignment of absolute stereochemistry.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.201200572

7 January 2021

inferred from DOI database lookup

Enantiomeric Relationships and Anthelmintic Activity of Dysinin Derivatives from Dysidea Marine Sponges

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.201200572

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/EJOC.201200572

1 reference

21 August 2017

1 reference

21 August 2017

PubMed publication ID

24653665

1 reference