Cart
Article
Keto-Enol Tautomers in a Carbonyl Phosphonium Salt
Hi-Res PDFPurchase the full-text
- PDF/HTML,
figures/images,
references and tables,
(where available)
Abstract
Supplementary NMR data is provided for an experiment previously published in this Journal describing the synthesis of carbonyl-stabilized ylides. The new data suggest that the keto-enol tautomerism is taking place in the phosphonium ion.
Keywords (Audience):
Upper-Division UndergraduateKeywords (Domain):
Inorganic ChemistryKeywords (Subject):
SynthesisCiting Articles
Citation data is made available by participants in CrossRef's Cited-by Linking service. For a more comprehensive list of citations to this article, users are encouraged to perform a search in SciFinder.
This article has been cited by 1 ACS Journal articles (1 most recent appear below).
Generation, Isolation, and Characterization of a Stable Enol from Grignard Addition to a Bis-Ester. A Microscale Experiment for the Undergraduate Organic Chemistry Laboratory
Olivier J.-C. Nicaise , Kyle F. Ostrom and Brent J. DalkeJournal of Chemical Education2005 82 (7), 1059Generation, Isolation, and Characterization of a Stable Enol from Grignard Addition to a Bis-Ester. A Microscale Experiment for the Undergraduate Organic Chemistry Laboratory
Olivier J.-C. Nicaise , Kyle F. Ostrom and Brent J. DalkeJournal of Chemical Education2005 82 (7), 1059A microscale experiment for the undergraduate organic chemistry laboratory that consists of preparing and characterizing an α-ketoester and its corresponding, remarkably stable enol form, has been developed. The reaction is that of a Grignard reagent with ...
Tools
-
Add to Favorites
-
Download Citation
-
Email a Colleague -
Permalink
Order Reprints
Rights & Permissions
Citation Alerts
History
- Received: August 03, 2009
ACS
Network
Facebook
Tweet This
CiteULike
Newsvine
Digg This
Delicious
C−(fc)n−C
