Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H6O |
| Molecular Weight | 82.1005 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCC=C1
InChI
InChIKey=BZKFMUIJRXWWQK-UHFFFAOYSA-N
InChI=1S/C5H6O/c6-5-3-1-2-4-5/h1,3H,2,4H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Lewis base effects in the Baylis-Hillman reaction of imines with cyclohex-2-en-1-one and cyclopent-2-en-1-one. | 2001 Sep 21 |
|
| The stereochemistry of the thermal cheletropic decarbonylation of 3-cyclopentenone as determined by multiphoton infrared photolysis/thermolysis. | 2003 Jul 16 |
|
| 2-Cyclopenten-1-one and prostaglandin J2 reduce restenosis after balloon angioplasty in rats: role of NF-kappaB. | 2003 Oct 9 |
|
| Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions. | 2004 Feb 6 |
|
| Stereoselective Nazarov cyclizations of bridged bicyclic dienones. | 2005 Jun 23 |
|
| Jet-cooled phosphorescence excitation spectrum of the T1(n,pi*) <-- S0 transition of 2-cyclopenten-1-one. | 2007 Aug 30 |
|
| Asymmetric Morita-Baylis-Hillman reaction of arylaldehydes with 2-cyclohexen-1-one catalyzed by chiral bis(thio)urea and DABCO. | 2008 Mar 20 |
|
| Gold-catalyzed hydrative carbocyclization of 1,5- and 1,6-diyn-3-ones via an oxygen transfer process. | 2008 Nov 7 |
|
| Identification of advanced reaction products originating from the initial 4-oxo-2-nonenal-cysteine Michael adducts. | 2009 May |
|
| Stereochemical and skeletal diversity arising from amino propargylic alcohols. | 2010 Jun 18 |
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DTXSID60870802
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930-30-3
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73117
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Cyclopentenone
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Q0U2IGF9CK
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213-213-0
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141550
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13588
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SUBSTANCE RECORD
