About: Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration

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About: Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration Goto Sponge NotDistinct Permalink

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scientific article published on 17 April 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2007 (uk) im April 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 17 April 2007 (en) գիտական հոդված հրատարակված 2007 թվականի ապրիլի 17-ին (hy) artículu científicu espublizáu n'abril de 2007 (ast)
publication date	wds:Q80169563-F0E5581D-461B-4CA3-A931-E398387952B3
publication date	2007-04-17 00:00:00Z (xsd:dateTime)
author name string	wds:Q80169563-5FD1CA62-E61D-409B-9341-DD27586BF47A wds:Q80169563-FD2CDD27-D4D4-4505-8AC7-C0CD35F267D6
author name string	Brandon I Morinaka Colin K Skepper
rdfs:label	Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (en) Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (nl)
skos:prefLabel	Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (en) Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (nl)
name	Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (en) Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (nl)
author	wds:Q80169563-58449653-1150-47AB-87B9-82819AD1531A
author	Tadeusz F. Molinski
title	wds:Q80169563-82171AF7-E3E5-456C-89C1-1496C06791A2
title	Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration (en)
page(s)	wds:Q80169563-BA665F4A-E39E-4B45-B9FE-A04101F1FCC9
page(s)	1975-1978
instance of	wds:Q80169563-126C96DF-E311-46A3-967F-989A2AC5217D
instance of	scholarly article
main subject	wds:Q80169563-104CB7F7-EC9D-4135-A2E9-C83E8BC9F6A2 wds:Q80169563-39286EE1-5383-4A68-8A35-53CC5EB45A69 wds:Q80169563-44657D9C-881D-4154-A8CA-99204AA40426 wds:Q80169563-54BF91B4-9DCD-49AA-88F7-3D51322761AE wds:Q80169563-60284F92-A8BA-4564-8602-14973991093A wds:Q80169563-62E35364-6189-40A1-A4D3-7B5C0DA1D934 wds:Q80169563-6C124E03-8127-4275-9D71-E26F57006053 wds:Q80169563-A5102735-6EAD-43D3-A02A-88ED29F3D0EB wds:Q80169563-A8E4E4C9-6CAE-47FC-8113-80A2400144B7 wds:Q80169563-B2924281-2DC0-454D-BC95-F220142F271B wds:Q80169563-B83E6CA8-E5B8-465B-A142-560561DF7355 wds:Q80169563-E3379C08-AF88-4073-B70F-0F4F1125437C
main subject	Xestospongia muta Mutafran E Mutafran A Mutafran F Mutafran B methyl (7E,9E,13E,15Z)-14,16-dibromohexadeca-7,9,13,15-tetraen-5-ynoate Methyl 14,16-dibromohexadeca-7,13,15-trien-5-ynoate Mutafran G Mutafran D Mutafran C Methyl 14,16-dibromohexadeca-7,9,13,15-tetraen-5-ynoate Methyl (7E,13E,15Z)-14,16-dibromohexadeca-7,13,15-trien-5-ynoate
PubMed ID	wds:Q80169563-E8C43387-006A-4ED5-B660-62208E683E8F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17439137
PubMed ID	17439137
published in	wds:Q80169563-06837228-DBBF-418A-ACB7-3B9B51B6C469
published in	Organic Letters
issue	wds:Q80169563-6248710D-DB97-4B85-BB8C-6E21793EF007
volume	wds:Q80169563-37D36F46-1B0A-43DE-A0E7-ECDCAC639DD8
issue	10
volume	9
DOI	wds:Q80169563-AF18F7D6-066F-43F7-A97E-2619F422C0A5
DOI	http://dx.doi.org/10.1021/OL0705696
DOI	10.1021/OL0705696
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80169563
is cites work of	Exciton coupling circular dichroism of an allylic N-imidazolyl group in amaranzole A, a marine natural product from Phorbas amaranthus Variations in Microbial Diversity and Metabolite Profiles of the Tropical Marine Sponge Xestospongia muta with Season and Depth Cobalt-Catalyzed 1,1-Diboration of Terminal Alkynes: Scope, Mechanism, and Synthetic Applications. Motualevic acids A-F, antimicrobial acids from the sponge Siliquariaspongia sp Synchronous bond molecular dynamics of conjugated chlorocyclopropyl alk-yn-enes revealed by ECD and UV-vis Liposomal Circular Dichroism (L-CD) of Arenoyl Derivatives of Sphingolipids. Amplification of Cotton Effects in Ordered Lipid Bilayers.
is cites work of	wds:Q58557316-C9EA35CD-B53C-4666-BDE1-9AE9359A84D0 wds:Q33893733-1B817D1D-69EB-4686-AFFE-686CEEDD2ACD wds:Q48234511-1E3540DF-23BB-4814-B916-1D76F1E9E0F1 wds:Q43211521-8B6850C4-0437-4244-A0E9-33EDAAD9B70A wds:Q96610296-5118E1AA-2CC8-42F5-9FC5-E9494BA408AA wds:Q50137813-C6452DFD-D05E-4ACC-ADED-171D4FC598B9
is pr:P248 of	wdref:25fea5ba986f29d77389e52ba448073966160e24

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