dc.contributor.author | Shanmugam, P | |
dc.contributor.author | Rajasingh, P | |
dc.date.accessioned | 2021-02-08T11:16:24Z | |
dc.date.available | 2021-02-08T11:16:24Z | |
dc.date.issued | 2005 | |
dc.identifier.citation | Chemistry Letters 34(11):1494-1495; 5 Nov 2005 | en_US |
dc.identifier.issn | 0366-7022 | |
dc.identifier.uri | http://hdl.handle.net/123456789/3647 | |
dc.description.abstract | An eco-friend method for the synthesis of 1-aryl indenes from Baylis-Hillman adducts using Mont. K10 and microwave combination as catalyst system and a procedure for the synthesis of beta- phenyl-substituted-protected Baylis-Hillman adducts with highly Z-selectivity have been reported. | en_US |
dc.language.iso | en | en_US |
dc.publisher | The Chemical Society of Japan | en_US |
dc.subject | 1-aryl indenes | en_US |
dc.subject | Baylis-Hillman adducts | en_US |
dc.subject | Montmorillonite K10 | en_US |
dc.subject | Allylic carbocation | en_US |
dc.title | Montmorillonite K10 clay-catalyzed synthesis of substituted 1-aryl indenes from Baylis-Hillman adducts | en_US |
dc.type | Article | en_US |