About: Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives

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scholarly article by H.A. Dieck & F.R. Heck published July 1975 in Journal of Organometallic Chemistry

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 1975 (uk) im Juli 1975 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by H.A. Dieck & F.R. Heck published July 1975 in Journal of Organometallic Chemistry (en)
publication date	wds:Q59700599-4FB773D0-9B0C-4DAA-A339-1F1C2CA56332
publication date	1975-07-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q59700599-193979E6-0343-42D4-922A-7B86098237E2 wds:Q59700599-574DC441-CA4A-4FEE-99D0-0284427AA722 wds:Q59700599-66A29B63-F3D1-4875-AE4B-81EF6F547F63 wds:Q59700599-8D296FA5-EDB6-4F17-BC88-4C59252515D3 wds:Q59700599-DF6861B3-73A2-46A8-B9E3-3B667D991108
cites work	Acylation, methylation, and carboxyalkylation of olefins by Group VIII metal derivatives Organophosphinepalladium complexes as catalysts for vinylic hydrogen substitution reactions Mechanism of arylation and carbomethoxylation of olefins with organopalladium compounds Mechanisms of Elimination Reactions. IX. The Spontaneous Decomposition of Salts of β-Halo Acids. II. trans-Cinnamic Acid Dibromide1 Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexes
author name string	wds:Q59700599-32B19CCB-A7BB-47AA-A1A9-BDCD3A4F2247 wds:Q59700599-F0AEFF5A-6919-41BD-81CD-0BF97FE35C85
author name string	F.R. Heck H.A. Dieck
rdfs:label	Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (en) Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (nl)
skos:prefLabel	Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (en) Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (nl)
name	Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (en) Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (nl)
title	wds:Q59700599-5BF5EF0D-EEFD-4924-B634-813D09CA68CE
title	Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives (en)
page(s)	wds:Q59700599-8DEB087F-D71C-49F3-BA5E-CCC8E7A127F1
page(s)	259-263
instance of	wds:Q59700599-28DE1DF3-94B9-449F-A9FF-CBE531854116
instance of	scholarly article
main subject	wds:Q59700599-F7117E5D-0456-4702-9D7F-B57A482C43E9
main subject	palladium
published in	wds:Q59700599-AEAC4D1A-828B-494E-AD37-EF18A272E7CC
published in	Journal of Organometallic Chemistry
issue	wds:Q59700599-B98E6C9B-083D-49AD-B463-8C4B272CAAA9
volume	wds:Q59700599-A1AB0819-31D7-4A05-AA27-FAECCE51EFD2
issue	2
volume	93
DOI	wds:Q59700599-1FC4A3FD-EF68-42C7-A9E9-D9E862E4D52B
DOI	http://dx.doi.org/10.1016/S0022-328X(00)94049-X
DOI	10.1016/S0022-328X(00)94049-X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59700599
is cites work of	Development of Pd–Cu catalyzed cross-coupling of terminal acetylenes with sp2-carbon halides A genealogy of Pd-catalyzed cross-coupling Palladium-catalyzed alkynylation. A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines A highly enantioselective intramolecular Heck reaction with a monodentate ligand Search for highly efficient, stereoselective, and practical synthesis of complex organic compounds of medicinal importance as exemplified by the synthesis of the C21-C37 fragment of amphotericin B. Kumada-Corriu reactions in a pressure-driven microflow reactor. Magical power of transition metals: past, present, and future (Nobel Lecture). Dendronized perylenetetracarboxdiimides with peripheral triphenylamines for intramolecular energy and electron transfer New synthesis of leukotriene B3 methyl ester from bis(trimethylsilyl) unsaturated derivatives 2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity. Elaboration of the side chain of α-amino acids containing a vinyl iodide by palladium-catalysed coupling Pd-EnCatTMTPP30 as a Catalyst for the Generation of Highly Functionalized Aryl- and Alkenyl-Substituted Acetylenes via Microwave-Assisted Sonogashira Type Reactions A Sustainable, User-Friendly Protocol for the Pd-Free Sonogashira Coupling Reaction A general asymmetric copper-catalysed Sonogashira C(sp3)-C(sp) coupling Highly substituted enyne formation by coupling reaction of alkenylzirconium compounds with alkynyl halides 2,5-Bis-(butyltelluro) thiophene as a convenient precursor for the synthesis of 2,5-bis-(acetylenic) thiophenes Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation Synthesis and anti-inflammatory activity of acetylenic thiophenes New acetylenic furan derivatives: synthesis and anti-inflammatory activity
is cites work of	wds:Q57718721-F5917AB1-800B-4497-94E6-7C7FE4FCAD97 wds:Q37896028-D5E9D7A2-1CB3-44DB-89CB-FFF89A572E7F wds:Q44736491-09E06E1E-0F3A-4E4B-BEC3-B0016FAC9E41 wds:Q56482569-5E25F900-95ED-4900-9509-15E1AB3C3925 wds:Q56592577-E7EF63D5-FB23-456D-9393-F1432120FE63 wds:Q57953385-C5AAD551-36E4-4C1A-B3D7-1CE4F35DF89B wds:Q37354967-932CE38E-799C-4BD1-BB25-1C3DE4F76267 wds:Q90859732-B0A62595-C64C-40AE-8656-8DB75B2CDA06 wds:Q35126603-9A8C77D5-D16B-49ED-8AD9-E2EC54B763F8 wds:Q48893643-20C88ECB-1C4A-4755-ACCC-9DDADA2F305E wds:Q60167020-21FA9F6A-5F12-45DC-8999-B8F8801C3EB8 wds:Q43848387-51402404-7F5D-4328-B154-E5A0412DC337 wds:Q56952219-293F7F68-7333-4069-B637-FC4790D9A464 wds:Q62745643-6E4B7715-B284-4B21-A171-D42B0EA98A4F wds:Q51597001-67C4EDE9-D777-45B4-8FFC-E25C6F906B3C wds:Q56484301-08D53431-E02F-4B95-A31B-C69F1F7E61E2 wds:Q62745796-C549BBC9-D2E9-4D89-9B54-B3DABCF1C15A wds:Q62745803-2D481E68-393A-4778-B1C8-4FAD0D4225AC wds:Q56028298-356301A2-1DA3-4235-8C73-F6CBA727A91D wds:Q59136626-15D5199B-0F9B-44DD-8E3C-C125C908E283

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