-
Nicholas J. (1969). "
Cyclopropanones".
Accounts of
Chemical Research. 2: 25–32. doi:10.1021/ar50013a004. De Kimpe, Norbert. "
Cyclopropanone".
Encyclopedia of...
- Lu, Ta-Jung (1987-10-28), Rappoport, Zvi (ed.), "The
Chemistry of
Cyclopropanones",
Cyclopropyl Group Volume 1 and
Volume 2 (1987), Chichester, UK: John...
- The
Favorskii rearrangement is prin****lly a
rearrangement of
cyclopropanones and α-halo
ketones that
leads to
carboxylic acid derivatives. In the case...
- "Isolation and
structure of coprine, a
novel physiologically active cyclopropanone derivative from
Coprinus atramentarius and its
synthesis via 1-aminocyclopropanol"...
-
Wiley & Sons, Inc. ISBN 978-1-119-24897-2. Salaun,
Jacques (1983). "
Cyclopropanone Hemiacetals".
Chemical Reviews. 83 (6): 619–632. doi:10.1021/cr00058a002...
-
simplest class have the
formula (CH2)nCO,
where n
varies from 2 for
cyclopropanone ((CH2)2CO) to the tens.
Larger derivatives exist.
Cyclohexanone ((CH2)5CO)...
- dichlorocyclopropanes.
These can be
reduced to
cyclopropanes or
hydrolysed to give
cyclopropanones by a
geminal halide hydrolysis.
Dichlorocyclopropanes may also be converted...
- (cycloalkanone). It is a
colorless volatile liquid at room temperature.
Since cyclopropanone is
highly sensitive,
cyclobutanone is the
smallest easily handled cyclic...
- This
reactive intermediate is
postulated to
occur in ring
opening of
cyclopropanones,
allene oxides and in the
Favorskii rearrangement. The intermediate...
-
readily because its
substituents are very small- a
purely steric effect.
Cyclopropanones- three-membered ring ketones- are also
hydrated to a
significant extent...
