About: Metal-centered cycloaddition reactions     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : dbo:Disease, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)
QRcode icon
http://dbpedia.demo.openlinksw.com/describe/?url=http%3A%2F%2Fdbpedia.org%2Fresource%2FMetal-centered_cycloaddition_reactions&invfp=IFP_OFF&sas=SAME_AS_OFF

A metal-centered cycloaddition is a subtype of the more general class of cycloaddition reactions. In such reactions "two or more unsaturated molecules unite directly to form a ring", incorporating a metal bonded to one or more of the molecules. Cycloadditions involving metal centers are a staple of organic and organometallic chemistry, and are involved in many industrially-valuable synthetic processes. For example, olefin metathesis using a Grubbs catalyst typically involves a reversible [2+2] cycloaddition. A Ruthenium alkylidene and an alkene (or alkyne) react to form a metallocycle.

AttributesValues
rdf:type
rdfs:label
  • Metal-centered cycloaddition reactions (en)
rdfs:comment
  • A metal-centered cycloaddition is a subtype of the more general class of cycloaddition reactions. In such reactions "two or more unsaturated molecules unite directly to form a ring", incorporating a metal bonded to one or more of the molecules. Cycloadditions involving metal centers are a staple of organic and organometallic chemistry, and are involved in many industrially-valuable synthetic processes. For example, olefin metathesis using a Grubbs catalyst typically involves a reversible [2+2] cycloaddition. A Ruthenium alkylidene and an alkene (or alkyne) react to form a metallocycle. (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/Cycloaddition_of_eta-6-Benzyltricarbonylmanganate_and_Diphenylketene.png
  • http://commons.wikimedia.org/wiki/Special:FilePath/Cycloadditionn_of_two_alkynes_to_form_a_Cyclobutadiene_ligand.png
  • http://commons.wikimedia.org/wiki/Special:FilePath/Dotz_benzannulation_reaction_diagram.png
  • http://commons.wikimedia.org/wiki/Special:FilePath/Formation_of_a_Ruthenium-phosphorous_metallocycle.png
  • http://commons.wikimedia.org/wiki/Special:FilePath/Photocatalyzed_5+4_cycloaddition.png
  • http://commons.wikimedia.org/wiki/Special:FilePath/Reaction_diagram_-_2+2_cycloaddition_of_Grubb's_Catalyst_with_Ethene.png
dcterms:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
sameAs
thumbnail
has abstract
  • A metal-centered cycloaddition is a subtype of the more general class of cycloaddition reactions. In such reactions "two or more unsaturated molecules unite directly to form a ring", incorporating a metal bonded to one or more of the molecules. Cycloadditions involving metal centers are a staple of organic and organometallic chemistry, and are involved in many industrially-valuable synthetic processes. There are two general types of metal-centered cycloaddition reactions: those in which the metal is incorporated into the cycle (a metallocycle), and those in which the metal is external to the cycle. These can be further divided into "true" cycloadditions (those that take place in a concerted fashion), and formal cycloadditions (those that take place in a stepwise fashion). Beyond that, they are classified by the number of atoms contributed to the cycle by each of the participants. For example, olefin metathesis using a Grubbs catalyst typically involves a reversible [2+2] cycloaddition. A Ruthenium alkylidene and an alkene (or alkyne) react to form a metallocycle. (en)
gold:hypernym
prov:wasDerivedFrom
page length (characters) of wiki page
foaf:isPrimaryTopicOf
is Link from a Wikipage to another Wikipage of
is foaf:primaryTopic of
Faceted Search & Find service v1.17_git139 as of Feb 29 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 08.03.3330 as of Mar 19 2024, on Linux (x86_64-generic-linux-glibc212), Single-Server Edition (378 GB total memory, 67 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software