About: Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091

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About: Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 Goto Sponge NotDistinct Permalink

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scientific article published on 04 September 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2012 (uk) artículu científicu espublizáu en setiembre de 2012 (ast) scientific article published on 04 September 2012 (en)
publication date	wds:Q84875878-4D5605C3-821C-471B-B68F-ECF4A6F299FE
publication date	2012-09-04 00:00:00Z (xsd:dateTime)
author name string	wds:Q84875878-6645E89C-D745-421D-AEDB-0BA61C700D5A wds:Q84875878-B0424A95-C282-4BD8-BAC6-E701FB8E4935 wds:Q84875878-DDB927B0-E34C-43CA-B2CF-9815B3CE1137
author name string	Caio C Oliveira Emerson A F dos Santos Julia H Bormio Nunes
rdfs:label	Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (en) Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (nl)
skos:prefLabel	Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (en) Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (nl)
name	Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (en) Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (nl)
author	wds:Q84875878-B859CD0F-F5E3-403F-B9B2-3EF94451F96F
author	Carlos Roque Duarte Correia
title	wds:Q84875878-0F919B36-D7E4-4D37-95F7-98CCE341DD9F
title	Stereoselective arylation of substituted cyclopentenes by substrate-directable Heck-Matsuda reactions: a concise total synthesis of the sphingosine 1-phosphate receptor (S1P(1)) agonist VPC01091 (en)
page(s)	wds:Q84875878-B0814EA4-BF7C-4D4E-B25C-8E103EA5F1D5
page(s)	8182-8190
instance of	wds:Q84875878-5ABCF9B7-3CAA-4475-96D2-635A30A720BA
instance of	scholarly article
main subject	wds:Q84875878-B226C483-6865-4A10-AB81-62399353B663
main subject	stereoselectivity
PubMed ID	wds:Q84875878-D3CC8815-4601-4D9D-8013-9287E57D498C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22924670
PubMed ID	22924670
published in	wds:Q84875878-F4E98820-EE37-407C-A7FD-5CB5FA0DC609
published in	Journal of Organic Chemistry
issue	wds:Q84875878-8BC07150-4ACA-434D-BE98-9594AAB0BFDE
volume	wds:Q84875878-A8A8922D-30CE-4F98-AD16-21F5E45CE733
issue	18
volume	77
DOI	wds:Q84875878-4CA09EF4-99B7-4627-B9CF-FAE5F46AD51A
DOI	http://dx.doi.org/10.1021/JO3015209
DOI	10.1021/JO3015209
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84875878
is cites work of	Enantioselective Heck-Matsuda Arylations through Chiral Anion Phase-Transfer of Aryl Diazonium Salts Triarylphosphine Ligands with Hemilabile Alkoxy Groups. Ligands for Nickel(II)-Catalyzed Olefin Dimerization Reactions. Hydrovinylation of Vi-nylarenes, 1,3-Dienes, and Cycloisomerization of 1,6-Dienes Palladium catalyzed heck arylation of 2,3-dihydrofuran-effect of the palladium precursor.
is cites work of	wds:Q41136749-28EACED6-8183-481A-AEA7-53CDA7D3B67F wds:Q34478311-167D8E13-6605-470D-9851-18E6E12BB4C2 wds:Q50804082-DE9252DF-6842-4EAF-B95A-B6ECDEA8C12E

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