About: Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine

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About: Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 2009

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique (publié 2009) (fr) наукова стаття, опублікована в січні 2009 (uk) im Jahr 2009 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2009 (ast) artikull shkencor i botuar më 01 janar 2009 (sq) scientific article published on 01 January 2009 (en)
publication date	wds:Q82735825-75F0CBFB-80B0-4719-BA7E-B9053052D75A
publication date	2009-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q82735825-6E6E94E5-CC03-4FA1-8AEC-50461BCF45D6
author name string	Manon Chaumontet
rdfs:label	Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (en) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (nl) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (sq)
skos:prefLabel	Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (en) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (nl) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (sq)
name	Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (en) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (nl) Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (sq)
author	wds:Q82735825-201C1EB0-FEB9-45F5-9E62-732CC215E5AE wds:Q82735825-5610184C-634D-4D10-A29F-8EB6A00715E1
author	Olivier Baudoin Riccardo Piccardi
title	wds:Q82735825-F1D988DB-0D76-4B5C-A663-B1055726DF37
title	Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: total synthesis of coralydine (en)
page(s)	wds:Q82735825-CA1F1490-3C41-432F-BFE0-BCF6675569E0
page(s)	179-182
instance of	wds:Q82735825-BDEB0107-4EE7-4C0B-B141-30A5EA7DD856
instance of	scholarly article
PubMed ID	wds:Q82735825-5AF65E82-249A-4018-B5E0-37FBC7B89CB5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19035607
PubMed ID	19035607
published in	wds:Q82735825-A44D70C9-B28A-421B-B35F-E755CB7E4039
published in	Angewandte Chemie International Edition
issue	wds:Q82735825-DFB9241E-E703-4B69-9D9B-7C5E50A39ADB
volume	wds:Q82735825-F37B7A64-4930-4D69-B66D-E0A2E0DBAE54
issue	1
volume	48
DOI	wds:Q82735825-F9274374-A06F-489F-BE73-BBA331455D1F
DOI	http://dx.doi.org/10.1002/ANIE.200804444
DOI	10.1002/ANIE.200804444
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q82735825
is cites work of	Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality Scope and limitations of auxiliary-assisted, palladium-catalyzed arylation and alkylation of sp2 and sp3 C-H bonds. Nonnatural amino acid synthesis by using carbon-hydrogen bond functionalization methodology Total synthesis of clostrubin Auxiliary-assisted palladium-catalyzed arylation and alkylation of sp2 and sp3 carbon-hydrogen bonds Palladium- and copper-catalyzed arylation of carbon-hydrogen bonds Mechanistic investigations and substrate scope evaluation of ruthenium-catalyzed direct sp3 arylation of benzylic positions directed by 3-substituted pyridines Synthesis of substituted isoquinolines utilizing palladium-catalyzed α-arylation of ketones. First selective direct mono-arylation of piperidines using ruthenium-catalyzed C-H activation.
is cites work of	wds:Q35245011-E8EA0DE0-F3F6-4317-9288-BC78CC439E5D wds:Q39818764-B47E4675-688D-4DC9-96FB-8506B13BB3F0 wds:Q42154000-7CB9037D-8A14-43E8-B3E5-F70BA669DF6A wds:Q42201427-1511DFD6-58B9-45E1-89E3-70A2E6B94C35 wds:Q37294999-2E194DED-27A4-4D5B-8813-8B500B64E764 wds:Q36122890-6710178D-12E2-40B2-88FD-28F3608842FA wds:Q40745800-DC1D1CF3-41EE-4949-B50B-271284B9CADF wds:Q33737426-D28286D3-CC51-4486-A89B-B4F731431B9E wds:Q42175339-44714D9D-8A18-4BE2-ADBF-E7FC28030777

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