About: A Concise Total Synthesis of the Notoamides C and D

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About: A Concise Total Synthesis of the Notoamides C and D Goto Sponge NotDistinct Permalink

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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:Q59710707-D691DD92-DD79-4542-BB43-3C32C7AD56B4
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59710707-6F5CF439-15CC-47A5-A10E-5D6080051E5A
language of work or name	English
cites work	wds:Q59710707-1CF7D683-F456-4405-BDF9-11A12CFA4DDB wds:Q59710707-68566794-A6FC-46CE-80E6-44371982A404 wds:Q59710707-B64A4FCB-1FFD-45A0-B873-6B5486DD36CD wds:Q59710707-BEC66623-51C9-4C69-854D-B26A99A71894
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 New paraherquamide antibiotics with anthelmintic activity
author name string	wds:Q59710707-11FA246E-93C4-46BE-9E8D-A385FF790EB6 wds:Q59710707-1D391676-A08B-4AB3-8768-5F027B8C4E14 wds:Q59710707-35903818-0B26-4641-852B-0085FE90B667
author name string	Robert M Williams Gerald D Artman Alan W Grubbs
rdfs:label	A Concise Total Synthesis of the Notoamides C and D (en) A Concise Total Synthesis of the Notoamides C and D (nl) A Concise Total Synthesis of the Notoamides C and D (sq)
skos:prefLabel	A Concise Total Synthesis of the Notoamides C and D (en) A Concise Total Synthesis of the Notoamides C and D (nl) A Concise Total Synthesis of the Notoamides C and D (sq)
name	A Concise Total Synthesis of the Notoamides C and D (en) A Concise Total Synthesis of the Notoamides C and D (nl) A Concise Total Synthesis of the Notoamides C and D (sq)
author	wds:Q59710707-4A2CFDEB-2883-46FD-B476-B12E2F81152D
author	Sachiko Tsukamoto
title	wds:Q59710707-3ACBA9EF-6F7E-446F-B77E-FD8A687F1109
title	A concise total synthesis of the notoamides C and D (en)
page(s)	wds:Q59710707-EB833019-41D3-41DE-8DE9-80CEEDCEBA0C
page(s)	2257-2261
instance of	wds:Q59710707-A61D65CC-2D38-4D83-BC47-9A9C9CA932A8
instance of	scholarly article
main subject	wds:Q59710707-37F02D6A-871B-4BC1-8234-7F4502CF10A8
main subject	general chemistry
PubMed ID	wds:Q59710707-58FA0333-1F01-48ED-A3B3-6AE5E0B8C39D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17304609
PubMed ID	17304609
published in	wds:Q59710707-CDB0D499-0C38-4D28-8B46-28DF6C199FAA
published in	Angewandte Chemie International Edition
issue	wds:Q59710707-C56459C3-DFFF-4432-808C-5006C53ECA48
volume	wds:Q59710707-3AA1F67E-CB82-471D-9544-A7F951464E35
issue	13
volume	46
DOI	wds:Q59710707-CE53BAF6-57FC-40FB-9993-C8F14B5DD84E
DOI	http://dx.doi.org/10.1002/ANIE.200604377
DOI	10.1002/ANIE.200604377
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59710707
is cites work of	Recent advances in the chemistry and biology of naturally occurring antibiotics Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis 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. Synthesis of notoamide J: a potentially pivotal intermediate in the biosynthesis of several prenylated indole alkaloids 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 Concise, Biomimetic Total Synthesis of d,l-Marcfortine C. Total synthesis and isolation of citrinalin and cyclopiamine congeners Distinct mechanisms for spiro-carbon formation reveal biosynthetic pathway crosstalk. Lessons and revelations from biomimetic syntheses Cycloexpansamines A and B: spiroindolinone alkaloids from a marine isolate of Penicillium sp. (SF-5292). Studies on Paraherquamide Biosynthesis: Synthesis of Deuterium-Labeled 7-Hydroxy-Pre-Paraherquamide, a Putative Precursor of Paraherquamides A, E & F Antifouling potentials of eight deep-sea-derived fungi from the South China Sea. Rational and combinatorial tailoring of bioactive cyclic dipeptides 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. An update on 2,5-diketopiperazines from marine organisms Oxidative reactions of tetrahydrobenzimidazole derivatives with N-sulfonyloxaziridines Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600. Synthesis and stereochemical determination of an antiparasitic pseudo-aminal type monoterpene indole alkaloid Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi Structure determination and total synthesis of (+)-16-hydroxy-16,22-dihydroapparicine 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 Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts.
is cites work of	wds:Q33351935-D8EEE5BF-97A4-495D-8FF7-630EECBAAE97 wds:Q33980370-74289D9A-CDA5-427D-9B70-EDAD77EA3354 wds:Q52603758-FFE64760-5A23-4D58-8816-060A133AB318 wds:Q37234744-93AF5238-20DF-497C-A3D9-BBAD2CBCDF5C wds:Q35580559-3C4322BC-4F7E-48E7-A1CD-DB92A425EFC2 wds:Q36854667-E20F62D8-E75A-4F98-8DC2-C11D47FE36CC wds:Q41925286-698D5259-FED5-4CAA-8129-8EBA4FB8F525 wds:Q42378249-7A09CDDA-1CBA-4520-A84F-63E4F0817263 wds:Q33750464-72D87699-77AB-4581-9673-273919FB7390

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