About: A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B

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scientific article published on 01 January 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique (publié 2007) (fr) наукова стаття, опублікована в березні 2007 (uk) im Jahr 2007 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2007 (ast) artikull shkencor i botuar më 01 janar 2007 (sq) scientific article published on 01 January 2007 (en)
publication date	wds:Q59710712-8ECA1C30-10FB-4ABB-BE06-FBA41203281D
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59710712-7F039ADA-1F92-4335-BA85-9E5A669DF4E6
language of work or name	English
cites work	wds:Q59710712-0EFCA1F6-510D-403B-A1FB-00A8CFD2C71E wds:Q59710712-10251B93-E546-4E78-AEF5-9DDE12E92930 wds:Q59710712-19264361-54BF-45ED-80F3-F10229B00C94 wds:Q59710712-7672E70B-6C74-4481-B22D-14F4A52B564F wds:Q59710712-9ED96F4E-52A6-4488-82DC-5723AA5B33BF
cites work	Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp Novel antinematodal and antiparasitic agents from Penicillium charlesii. II. Structure determination of paraherquamides B, C, D, E, F, and G. Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity A new antibiotic CJ-17,665 from Aspergillus ochraceus. Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides
author name string	wds:Q59710712-02C05C21-F324-4CAB-9512-9C235243365B wds:Q59710712-CDA1FFE4-9EDB-404B-9DA0-F61778D50745 wds:Q59710712-D37FEC5E-6EB1-4DF3-A1C2-6EDAD897E782
author name string	Robert M Williams Thomas J Greshock Alan W Grubbs
rdfs:label	A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (en) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (nl) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (sq)
skos:prefLabel	A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (en) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (nl) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (sq)
name	A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (en) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (nl) A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B (sq)
author	wds:Q59710712-6E090F57-8FF1-4A22-AFC3-B0B45D4172D0
author	Sachiko Tsukamoto
title	wds:Q59710712-74D42DF6-08BB-47C8-8D89-291F3E47E3BB
title	A concise, biomimetic total synthesis of stephacidin A and notoamide B (en)
page(s)	wds:Q59710712-35CBE7CB-1F32-419B-83C9-13498A6AA2B3
page(s)	2262-2265
instance of	wds:Q59710712-BEBBBEEB-08EB-4817-9B8C-B22599014039
instance of	scholarly article
main subject	wds:Q59710712-FE49B9F8-D261-44E1-BC16-A4CF92B0C43A
main subject	general chemistry
PubMed ID	wds:Q59710712-D60436D9-019A-4154-9626-17EB52799E84
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17304610
PubMed ID	17304610
published in	wds:Q59710712-6E9EAE23-C13E-421A-B109-FD81134654F0
published in	Angewandte Chemie International Edition
issue	wds:Q59710712-0C0CEEB6-2FC7-4AB4-A658-08A8EA7262BC
volume	wds:Q59710712-BF63BD87-F3B8-448E-B9CB-2A0EE0E4FBC8
issue	13
volume	46
DOI	wds:Q59710712-5D71BCE8-580C-49A0-AE45-0EE7D9D045DF
DOI	http://dx.doi.org/10.1002/ANIE.200604378
DOI	10.1002/ANIE.200604378
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59710712
is cites work of	Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp Isolation of notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp Studies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic Conundrum Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600. Biomimetic total synthesis of malbrancheamide and malbrancheamide B Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications Isolation of antipodal (-)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp. STUDIES ON THE BIOSYNTHESIS OF THE STEPHACIDINS AND NOTOAMIDES. TOTAL SYNTHESIS OF NOTOAMIDE S. Concise, asymmetric, stereocontrolled total synthesis of stephacidins A, B and notoamide B Calmodulin inhibitory activity of the malbrancheamides and various analogs. Premalbrancheamide: synthesis, isotopic labeling, biosynthetic incorporation, and detection in cultures of Malbranchea aurantiaca Concise, Biomimetic Total Synthesis of d,l-Marcfortine C. Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids Enantioselective total synthesis of (-)-citrinadin A and revision of its stereochemical structure Enantioselective total syntheses of citrinadins A and B. Stereochemical revision of their assigned structures. Rapid access to spirocyclic oxindole alkaloids: application of the asymmetric palladium-catalyzed [3 + 2] trimethylenemethane cycloaddition Lessons and revelations from biomimetic syntheses Studies on Paraherquamide Biosynthesis: Synthesis of Deuterium-Labeled 7-Hydroxy-Pre-Paraherquamide, a Putative Precursor of Paraherquamides A, E & F Anti-proliferative activity of the NPM1 interacting natural product avrainvillamide in acute myeloid leukemia. Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J. Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E. Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600. Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide Natural products synthesis: enabling tools to penetrate Nature's secrets of biogenesis and biomechanism Oxidative reactions of tetrahydrobenzimidazole derivatives with N-sulfonyloxaziridines Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I. Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600. Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi Studies Towards Paraherquamides E & F and Related C-labeled Putative Biosynthetic Intermediates: Stereocontrolled Synthesis of the α-Alkyl-β-Methylproline Ring System Enzyme evolution in fungal indole alkaloid biosynthesis A unified strategy to reverse-prenylated indole alkaloids: total syntheses of preparaherquamide, premalbrancheamide, and (+)-VM-55599 Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts. Further Investigation of the Intermolecular Diels-Alder Cycloaddition for the Synthesis of Bicyclo[2.2.2]diazaoctane Alkaloids.
is cites work of	wds:Q33351935-32F7F7A3-0A7A-46ED-AA55-99EDA9A227DD wds:Q33731803-64AB26C4-E55D-4A7F-883E-6B90EFECFE8E wds:Q52603758-8063F226-80A9-45E0-A177-5DCECA5B94CE

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