Radical Cyclization of Exo-Methylene Furanose Derivatives: an Expedient approach to the Synthesis of Chiral Tricyclic Nucleosides and Benzannulated Oxepine Derivatives.
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
Radical Cyclization of Exo-Methylene Furanose Derivatives: an Expedient approach to the Synthesis of Chiral Tricyclic
Nucleosides and Benzannulated Oxepine Derivatives.
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| Creator |
Neogi, Arpita
Majhi, Tirtha Pada Ghoshal, Nanda Chattopadhyay, Partha |
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| Subject |
Chemistry
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| Description |
Abstract—Tributyltin radical mediated cyclization of the glucose derived exo-methylene furanose derivatives 5a–c led to the highly
functionalized cis-fused bicyclic ethers 6a–c. The product could subsequently be transformed to the optically active tricyclic nucleoside
analogue 8 or oxepine derivative 9.
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| Publisher |
Elsevier
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| Date |
2005
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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/330/1/TETRAHEDRON_61(_39)_9368%2D93742005[19].pdf
Neogi, Arpita and Majhi, Tirtha Pada and Ghoshal, Nanda and Chattopadhyay, Partha (2005) Radical Cyclization of Exo-Methylene Furanose Derivatives: an Expedient approach to the Synthesis of Chiral Tricyclic Nucleosides and Benzannulated Oxepine Derivatives. Tetrahedron, 61 (39). pp. 9368-9374. |
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| Relation |
http://dx.doi.org/10.1016/j.tet.2005.07.054
http://www.eprints.iicb.res.in/330/ |
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