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An Efficient Synthesis of Novel Dibenzo-Fused Nine-Membered Oxacycles Using a Sequential Baylis–Hillman Reaction and Radical Cyclization
EPrints@IICB
View Archive Info| Field | Value | |
| Title |
An Efficient Synthesis of Novel Dibenzo-Fused Nine-Membered Oxacycles Using a Sequential Baylis–Hillman Reaction and Radical Cyclization
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| Creator |
Majhi, Tirtha Pada
Neogi, Arpita Ghosh, Soumen Mukherjee, Alok Kumar Helliwell, Madeleine Chattopadhyay, Partha |
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| Subject |
Chemistry
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| Description |
A short and high yield synthetic route to novel dibenz[b,g]oxonins, one of which has been characterized by X-ray crystallography, has been developed based on a sequential Baylis– Hillman reaction and radical cyclization. The regioselective radical cyclization followed a 9-endo-trig pathway. |
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| Date |
2008
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://www.eprints.iicb.res.in/183/1/SYNTHESIS%2DSTUTTGART%2C_1%2C_94%2D100%2C2008[138].pdf
Majhi, Tirtha Pada and Neogi, Arpita and Ghosh, Soumen and Mukherjee, Alok Kumar and Helliwell, Madeleine and Chattopadhyay, Partha (2008) An Efficient Synthesis of Novel Dibenzo-Fused Nine-Membered Oxacycles Using a Sequential Baylis–Hillman Reaction and Radical Cyclization. Synthese, 1. pp. 94-100. |
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| Relation |
http://dx.doi.org/10.1055/s-2007-1000827
http://www.eprints.iicb.res.in/183/ |
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