An Easy Access to Spiroannulated Glyco-Oxetane, -thietane and -azetane Rings: Synthesis of Spironucleosides
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
An Easy Access to Spiroannulated Glyco-Oxetane, -thietane
and -azetane Rings: Synthesis of Spironucleosides
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| Creator |
Roy, Ashim
Achari, Basudeb Mandal, Sukhendu B |
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| Subject |
Chemistry
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| Description |
The key intermediate 11 derived from D-glucose and possessing bis-mesylmethyl (MsOÆCH2–) functionality at C-4, was used to generate spirocycles 12, 13 and 15 via one-step procedures. The spirocompounds 12 and 13 were subsequently converted into the corresponding spironucleosides 24 and 26 in good yield using Vorbru¨ggen reaction conditions.
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| Date |
2006
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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/1110/1/TETRAHEDRON_LETTERS__Volume_47___Issue_23___Pages_3875%2D3879___[78].pdf
Roy, Ashim and Achari, Basudeb and Mandal, Sukhendu B (2006) An Easy Access to Spiroannulated Glyco-Oxetane, -thietane and -azetane Rings: Synthesis of Spironucleosides. Tetrahedron Letters, 47 (23). pp. 3875-3879. |
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| Relation |
http://dx.doi.org/10.1016/j.tetlet.2006.03.175
http://www.eprints.iicb.res.in/1110/ |
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