About: Bradsher cycloaddition   Goto Sponge  NotDistinct  Permalink

An Entity of Type : yago:Process100029677, within Data Space : wasabi.inria.fr associated with source document(s)

The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium. The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958.

AttributesValues
type
label
  • Bradsher cycloaddition
  • Reacció de cicloaddició de Bradsher
comment
  • La cicloaddició de Bradsher , en química, és una forma de la reacció de Diels-Alder que implica l'addició [4+2] d'un dienòfil amb aromàtics catiònics xom és l'acridizini o . La cicloaddició de Bradsher va ser donada a conèixer per C. K. Bradsher i T. W. G. Solomons en la revista Journal of the American Chemical Society de l'American Chemical Society el 1958.
  • The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium. The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958.
sameAs
topic
depiction
  • External Image
described by
subject
dbo:wikiPageID
Wikipage revision ID
dbo:wikiPageWikiLink
is primary topic of
wasDerivedFrom
http://purl.org/li...ics/gold/hypernym
dbo:abstract
  • La cicloaddició de Bradsher , en química, és una forma de la reacció de Diels-Alder que implica l'addició [4+2] d'un dienòfil amb aromàtics catiònics xom és l'acridizini o . La cicloaddició de Bradsher va ser donada a conèixer per C. K. Bradsher i T. W. G. Solomons en la revista Journal of the American Chemical Society de l'American Chemical Society el 1958.
  • The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium. The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958.
dbo:thumbnail
dbo:wikiPageLength
dbp:wikiPageUsesTemplate
is sameAs of
is topic of
is dbo:wikiPageWikiLink of
is Wikipage disambiguates of
is topic of
is http://vocab.deri.ie/void#inDataset of
Faceted Search & Find service v1.13.91 as of Mar 24 2020


Alternative Linked Data Documents: Sponger | ODE     Content Formats:       RDF       ODATA       Microdata      About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data]
OpenLink Virtuoso version 07.20.3229 as of Jul 10 2020, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (94 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software