About: Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry

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scholarly article by Matthew Ball et al published 26 August 2005 in Angewandte Chemie International Edition

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в серпні 2005 (uk) im August 2005 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Matthew Ball et al published 26 August 2005 in Angewandte Chemie International Edition (en)
publication date	wds:Q56952556-1E69C542-AE93-4F6F-8509-7B66EB46AD8C
publication date	2005-08-26 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56952556-B2E7D4DF-AE11-4F11-9BC6-ADCEA145DEA6
language of work or name	English
cites work	wds:Q56952556-504DFFBB-5423-4F25-983A-D2BF93601588 wds:Q56952556-94F5B754-4514-4876-BCD8-A9A14766DA63
cites work	Marine Natural Products. XXXVIII. Absolute Stereostructures of Altohyrtins A, B, and C and 5-Desacetylaltohyrtin A, Potent Cytotoxic Macrolides, from the Okinawan Marine Sponge Hyrtios altum. Altohyrtins B and C and 5-desacetylaltohyrtin A, potent cytotoxic macrolide congeners of altohyrtin A, from the Okinawan marine sponge Hyrtios altum
author name string	wds:Q56952556-0D5347C9-E1BE-4D4B-AFC1-F09AEAEBDBC7 wds:Q56952556-334E923D-B372-48A3-B6FB-04B84A35B990 wds:Q56952556-413709AD-C8D5-48B8-A30C-62E1ADE22785 wds:Q56952556-4E386BCF-A67D-420A-983B-81718968502A wds:Q56952556-6F820D3C-0608-41E2-8062-4BB90F61B1F4 wds:Q56952556-73FDDF8A-3CBD-43E3-BF90-2473A20E9237 wds:Q56952556-941DC4F5-92D1-4656-ADBE-318A1A14E977 wds:Q56952556-9497589A-417F-4844-A576-2BD831C432BA wds:Q56952556-BA0318FA-E9C0-41CB-AF5F-9E2127DCD92F
author name string	Paolo Orsini Alessandra Scolaro Matthew Ball Shigeo Yamanoi Adam C. Talbot Alan S. Jessiman David F. Hook Huw R. Tanner Shigeru Kawahara
rdfs:label	Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (en) Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (nl)
skos:prefLabel	Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (en) Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (nl)
name	Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (en) Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (nl)
author	wds:Q56952556-2B6C99F8-84C1-4FFD-86C9-F2FF10A47E70 wds:Q56952556-709FC494-63E4-4B5A-91B8-5B81AE9317C1
author	Steven V. Ley Matthew J. Gaunt
title	wds:Q56952556-E66DA910-C4BE-4678-B7A8-37326097CBE9
title	Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry (en)
page(s)	wds:Q56952556-07C5A304-5084-4D73-B030-CD4FEAF65D6D
page(s)	5433-5438
instance of	wds:Q56952556-DDD2F8BD-C229-4C8D-973A-4E258C67847C
instance of	scholarly article
main subject	wds:Q56952556-1118EC90-9298-4078-9AD8-2BF801EA86CC wds:Q56952556-839F18BD-9FB7-4719-B7E3-B35B81A4BB62
main subject	general chemistry catalysis
PubMed ID	wds:Q56952556-D972F247-C9F2-4B75-B046-32737501F244
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16059947
PubMed ID	16059947
published in	wds:Q56952556-ECA6370B-BF7F-4003-B49E-6B456CE7804D
published in	Angewandte Chemie International Edition
issue	wds:Q56952556-8427F553-00A0-4DE1-8872-A0B2BDAF92DE
volume	wds:Q56952556-7B2606BD-9B6E-4029-9D78-3D2217BF3E7E
issue	34
volume	44
DOI	wds:Q56952556-A4ABB420-5E62-4A14-982E-EE021EA270BC
DOI	http://dx.doi.org/10.1002/ANIE.200502008
DOI	10.1002/ANIE.200502008
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56952556
is cites work of	Conformation-activity relationships of polyketide natural products Natural-product-like spiroketals and fused bicyclic acetals as potential therapeutic agents for B-cell chronic lymphocytic leukaemia Natural product synthesis in the age of scalability Gram-scale synthesis of (+)-spongistatin 1: development of an improved, scalable synthesis of the F-ring subunit, fragment union, and final elaboration Spongipyran Synthetic Studies. Evolution of a Scalable Total Synthesis of (+)-Spongistatin 1 Toward a more step-economical and scalable synthesis of spongistatin 1 to facilitate cancer drug development efforts Complex fragment coupling by crotylation: A powerful tool for polyketide natural product synthesis Spongipyran Synthetic Studies. Total Synthesis of (+)-Spongistatin 2. Exploiting pseudo C2-symmetry for an efficient synthesis of the F-ring of the spongistatins Hydroxyl-directed stereoselective diboration of alkenes. Enantioselective functionalization of allylic C-H bonds following a strategy of functionalization and diversification Design, synthesis, and biological evaluation of diminutive forms of (+)-spongistatin 1: lessons learned Recent synthetic approaches toward non-anomeric spiroketals in natural products. The medicinal potential of promising marine macrolides with anticancer activity [Search for natural substances with therapeutic activity: George R. Pettit]. Synthesis of spongistatin 2 employing a new route to the EF fragment Structure determination and total synthesis of (+)-16-hydroxy-16,22-dihydroapparicine Design, synthesis, and biological evaluation of EF- and ABEF- analogues of (+)-spongistatin 1 Design and 22-step synthesis of highly potent D-ring modified and linker-equipped analogs of spongistatin 1 Mechanistic investigations on Pinnick oxidation: a density functional theory study Synthesis of the northern sector (C8-C19) of rapamycin via Chan rearrangement and oxidation of an alpha-acyloxyacetate
is cites work of	wds:Q33386325-A79555DB-B12D-48AB-81F0-6F1462908876 wds:Q37352909-50F281FA-7C83-440B-9337-8B3383A1D9E6 wds:Q37548669-FA98DD02-0F10-4D96-A8BF-6A8C2B9D146A wds:Q34081227-87FA0FBA-8626-46C3-A9DB-6CC72CFC4B50 wds:Q52335669-35B65B38-DBFC-403B-8376-5CB8106BB062 wds:Q56951744-CD82B0A2-F6F2-4AC2-8FB5-B83890DBDC93 wds:Q41925286-983F504D-0E5A-4799-8981-54E515DB7FD9 wds:Q37837738-0488C5CE-B5AF-4F95-ABD3-19EDB7A0534D wds:Q39726213-EC76360C-0C58-4DE5-8EC8-1E0E80507A66 wds:Q38171270-D2666A13-9021-448A-833D-1D26C4C17DD0 wds:Q38279846-AADA8B6F-734F-4A7D-883C-DB9833AD0E52 wds:Q58568333-14F23796-BE9D-4583-B8D2-D543C7C427F5 wds:Q34081544-FF121ABA-55FE-473E-BFF1-DA68CAD96CFB wds:Q33642766-B64B43D1-4CA0-49EA-B4D4-30D71A06EC38

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