About: Total Synthesis and Complete Stereostructure of Gambieric Acid A

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article by Haruhiko Fuwa et al published 16 July 2012 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована в липні 2012 (uk) im Juli 2012 veröffentlichter wissenschaftlicher Artikel (de) article by Haruhiko Fuwa et al published 16 July 2012 in Journal of the American Chemical Society (en)
publication date	wds:Q57521114-039DB240-2777-48DB-855E-2EA9D35CA568
publication date	2012-07-16 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57521114-1D752429-2ABD-4945-88E9-1FF20E9771C8
language of work or name	English
cites work	wds:Q57521114-8B6A47EF-1234-4284-A9BE-0675F6B2D612
cites work	Biological activities of novel polyether antifungals, gambieric acids A and B from a marine dinoflagellate Gambierdiscus toxicus
author name string	wds:Q57521114-6EBA7718-49FB-4F1B-A143-9A2F73DF34FE wds:Q57521114-BE711FB3-FA71-47E6-B2D5-F18769E2E23C wds:Q57521114-E020C019-A225-446C-B5AC-47D03334063B
author name string	Makoto Sasaki Kazuya Ishigai Keisuke Hashizume
rdfs:label	Total Synthesis and Complete Stereostructure of Gambieric Acid A (en) Total Synthesis and Complete Stereostructure of Gambieric Acid A (nl)
skos:prefLabel	Total Synthesis and Complete Stereostructure of Gambieric Acid A (en) Total Synthesis and Complete Stereostructure of Gambieric Acid A (nl)
name	Total Synthesis and Complete Stereostructure of Gambieric Acid A (en) Total Synthesis and Complete Stereostructure of Gambieric Acid A (nl)
author	wds:Q57521114-F3FC0147-31DF-4982-B5E6-7FF4D060341C
author	Haruhiko Fuwa
title	wds:Q57521114-D94A7A83-7707-4DE2-92D2-C58B908B97EF
title	Total Synthesis and Complete Stereostructure of Gambieric Acid A (en)
page(s)	wds:Q57521114-9B96552C-F841-4EA3-88C9-3B4D294788C3
page(s)	11984-11987
instance of	wds:Q57521114-1083333E-149B-4983-9D46-76956CD50E8F
instance of	scholarly article
PubMed ID	wds:Q57521114-654EA9B6-E36B-4BCF-B509-426BBF7A8844
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22779404
PubMed ID	22779404
published in	wds:Q57521114-8F82D14D-1B47-4AAE-B575-1F5EB025A3B2
published in	Journal of the American Chemical Society
issue	wds:Q57521114-F7A8EA02-F79F-44A7-816C-7EE25BC496B6
volume	wds:Q57521114-42984F37-6C07-412F-9D1D-6005C2738E67
issue	29
volume	134
DOI	wds:Q57521114-D39FDE38-3F2B-4E53-939D-E5D70AB8E391
DOI	http://dx.doi.org/10.1021/JA305864Z
DOI	10.1021/JA305864Z
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57521114
is cites work of	Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product Total synthesis and biological evaluation of (+)-gambieric acid A and its analogues. Total synthesis, stereochemical reassignment, and biological evaluation of (-)-lyngbyaloside B. Misassigned natural products and their revised structures Identification of ciguatoxins in a shark involved in a fatal food poisoning in the Indian Ocean. Total Synthesis and Complete Stereostructure of a Marine Macrolide Glycoside, (-)-Lyngbyaloside B. Total synthesis and complete structural assignment of gambieric acid A, a large polycyclic ether marine natural product Concise synthesis of the A/BCD-ring fragment of gambieric acid A. Biotechnological and Pharmacological Applications of Biotoxins and Other Bioactive Molecules from Dinoflagellates. Methods for determining the absolute configurations of marine ladder-shaped polyethers Synthesis of α,α'-trans-oxepanes through an organocatalytic oxa-conjugate addition reaction Stereoelectronic Model To Explain Highly Stereoselective Reactions of Seven-Membered-Ring Oxocarbenium-Ion Intermediates Ciguatera Mini Review: 21st Century Environmental Challenges and the Interdisciplinary Research Efforts Rising to Meet Them
is cites work of	wds:Q26749672-5E77DAAF-2D31-434D-B531-90FE1DDCB4B5 wds:Q38940745-151A0FB8-A717-416D-9AE5-1B47DD6D3DEF wds:Q43104102-220FB7E6-F6EA-4646-9310-BC849A89E4EB wds:Q89744225-8D474A54-BA5B-472C-918F-C4CE7A756E06 wds:Q33598864-DA6A957F-E9F0-48F0-B92F-EA8A94F491DD wds:Q39823734-29C2B2DB-2C38-42C2-A868-0171E6BAFDCE wds:Q36738031-029C8730-781F-4307-B52C-7F1C765B3822 wds:Q38574438-85A5AA36-A8EC-43E3-A5A9-38CF55FC6521 wds:Q47231970-FC3787A7-7394-4314-BF97-0C12CD8EFABD wds:Q111152397-99D807E4-BDAE-45ED-B92A-26FF562C45B1 wds:Q38236979-265BD85E-FC7F-48F6-AEDF-81D5E5FA20AD wds:Q53113205-C32544F7-33F5-4720-96FC-B70FF5C75022 wds:Q41356826-C79399E0-E80F-404F-BCC5-CA5A0A1EFE32

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