Synthesis of chiral cis- and trans-furo[3,2-c][2]benzoxocines from D-glucose by regioselective 8-endo aryl radical cyclisation
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
Synthesis of chiral cis- and trans-furo[3,2-c][2]benzoxocines from D-glucose by regioselective 8-endo aryl radical cyclisation
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| Creator |
Nandi, Aniruddha
Mukhopadhyay, Ranjan Chattopadhyay, Partha |
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| Subject |
Chemistry
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| Description |
A simple chiral synthesis of cis- and trans-furo[3,2-c][2]benzoxocines 8a–d and 9a–d through a regioselective
8-endo-trig aryl radical cyclisation of the respective 5,6-dideoxy--xylo-hex-5-enofuranosides 6a–d and
5,6-dideoxy--ribo-hex-5-enofuranosides 7a–d with tributyltin hydride is described.
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| Date |
2001
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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/881/1/JOURNAL_OF_THE_CHEMICAL_SOCIETY%2DPERKIN_TRANSACTIONS_1%2C_24%2C_3346%2D3351%2C2001[75].pdf
Nandi, Aniruddha and Mukhopadhyay, Ranjan and Chattopadhyay, Partha (2001) Synthesis of chiral cis- and trans-furo[3,2-c][2]benzoxocines from D-glucose by regioselective 8-endo aryl radical cyclisation. Journal of Chemical Society- Perkin Transactions, 1 (24). pp. 3346-3351. |
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| Relation |
http://dx.doi.org/10.1039/B107886K
http://www.eprints.iicb.res.in/881/ |
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