ORTHO-VANILLYL ALCOHOL AS A SYNTHETIC EQUIVALENT OF 2-METHOXYCYCLOHEXA-2,4-DIENONES - A NOVEL SYNTHESIS OF LINEARLY FUSED CIS-ANTI-CIS-TRICYCLOPENTANOIDS
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Title |
ORTHO-VANILLYL ALCOHOL AS A SYNTHETIC EQUIVALENT OF 2-METHOXYCYCLOHEXA-2,4-DIENONES - A NOVEL SYNTHESIS OF LINEARLY FUSED CIS-ANTI-CIS-TRICYCLOPENTANOIDS
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Creator |
SINGH, V
THOMAS, B |
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Subject |
mediated cyclization reaction
(+/-)-hirsutene photochemistry oxidation ketones phenols beta |
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Description |
A novel and efficient synthesis of tricyclopentanoids via inverse demand pi-4s + pi-2s cycloaddition and photochemical reaction of annulated[2.2.2]octenones having an alpha-alkoxy-beta,gamma-unsaturated carbonyl chromophore, is described.
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Publisher |
ROYAL SOC CHEMISTRY
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Date |
2011-08-28T15:31:45Z
2011-12-26T12:58:05Z 2011-12-27T05:47:20Z 2011-08-28T15:31:45Z 2011-12-26T12:58:05Z 2011-12-27T05:47:20Z 1992 |
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Type |
Article
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Identifier |
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, (17), 1211-1213
0022-4936 http://dx.doi.org/10.1039/c39920001211 http://dspace.library.iitb.ac.in/xmlui/handle/10054/11774 http://hdl.handle.net/10054/11774 |
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Language |
en
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