Synthesis of Chiral Trans-Fused Pyrano[3,2-c][2]Benzoxocines from D-mannose by Regioselective 8-endo-Aryl radical Cyclization
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
Synthesis of Chiral Trans-Fused Pyrano[3,2-c][2]Benzoxocines from
D-mannose by Regioselective 8-endo-Aryl radical Cyclization
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| Creator |
Nandi, Aniruddha
Chattopadhyay, Partha |
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| Subject |
Chemistry
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| Description |
A simple chiral synthesis of trans-pyrano[3,2-c][2]benzoxocines 8a–d in good yields (60–75%) through regioselective
8-endo-trig aryl radical cyclization of the D-mannose derived enopyranosides 7a–d with Bu3SnH is described. © 2002 Elsevier
Science Ltd. All rights reserved.
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| Publisher |
Elsevier
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| Date |
2002
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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/789/1/TETRAHEDRON_LETTERS___43_(34)5977%2D5980;2002[33].pdf
Nandi, Aniruddha and Chattopadhyay, Partha (2002) Synthesis of Chiral Trans-Fused Pyrano[3,2-c][2]Benzoxocines from D-mannose by Regioselective 8-endo-Aryl radical Cyclization. Tetrahedron Letters, 43 (34). pp. 5977-5980. |
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| Relation |
http://dx.doi.org/10.1016/S0040-4039(02)01252-2
http://www.eprints.iicb.res.in/789/ |
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