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DC Field | Value | Language |
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dc.contributor.author | Anas, S | - |
dc.contributor.author | Jubi John | - |
dc.contributor.author | Sajisha, V S | - |
dc.contributor.author | Joshni John | - |
dc.contributor.author | Rani Rajan | - |
dc.contributor.author | Suresh, E | - |
dc.contributor.author | Radhakrishnan, K V | - |
dc.date.accessioned | 2011-03-14T09:28:50Z | - |
dc.date.available | 2011-03-14T09:28:50Z | - |
dc.date.issued | 2007 | - |
dc.identifier.citation | Organic and Biomolecular Chemistry 5:4010-4019;2007 | en_US |
dc.identifier.other | 150-2007 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/57 | - |
dc.description.abstract | A Novel reactivity of organoboronic acids with bicyclic hydrazines leading to the stereoselective formation of trans-vicinal disubstituted cyclopentenes in good to excellent yield is discussed. The reaction of cyclopentadiene and fulvene derived azabicyclic alkenenes with organoboronic acids afforded the trans-3,4-disubstituted cyclopentenes and alkylidene cyclopentenes in good to excellent yields. The products, having a broad range of substituents, are important intermediated in the synthesis of a number of pharmaceutically important molecules. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry, London | en_US |
dc.subject | Palladium catalyzed ring | en_US |
dc.subject | Azabicyclic olefins | en_US |
dc.subject | Hydrazinocyclopentene | en_US |
dc.title | Iodine assisted palladium catalyzed ring opening of bicyclic hydrazines with organoboronic acids: Sereoselective synthesis of functionalized cyclopentenes and alkylidene cyclopentenes | en_US |
dc.type | Article | en_US |
niist.citation | - | |
Appears in Collections: | 2007 |
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File | Description | Size | Format | |
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2007_00150.pdf Restricted Access | 195.73 kB | Adobe PDF | View/Open Request a copy |
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