uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Stepwise and concerted solvolytic elimination and substitution reactions: E1 reaction via a primary carbocation
Uppsala University.
Uppsala University.
1997 (English)In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol. 119, no 21, 4834-4840 p.Other (Other scientific)
Abstract [en]

Solvolysis of 9-(X-methyl)fluorene (1-X, X = I, Br, OBs) in 25 vol % acetonitrile in water gives the elimination product 9-methylidenefluorene and the substitution products 9-(hydroxymethyl)fluorene (1-OH) and 9-(acetamidomethyl)fluorene (1-NHCOMe). Kine

Place, publisher, year, pages
AMER CHEMICAL SOC , 1997. Vol. 119, no 21, 4834-4840 p.
Keyword [en]
PROMOTED E2 REACTION; AQUEOUS SOLVENT; BASE CATALYSIS; ION-PAIRS; MECHANISMS; DERIVATIVES; BORDERLINE; DEPROTONATION
Identifiers
URN: urn:nbn:se:uu:diva-78896OAI: oai:DiVA.org:uu-78896DiVA: diva2:106809
Note
Addresses: UNIV UPPSALA, INST CHEM, S-75121 UPPSALA, SWEDEN.Available from: 2008-10-17 Created: 2008-10-17

Open Access in DiVA

No full text

By organisation
Uppsala University

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 459 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf