Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring systems by endo-selective 2-pyridyl radical cyclizations
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring
systems by endo-selective 2-pyridyl radical cyclizations
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| Creator |
Maiti, Sarbendu
Achari, Basudeb Mukhopadhyay, Ranjan Banerjee, Asish Kr |
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| Subject |
Chemistry
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| Description |
Bu3SnH-induced 2-pyridyl radicals, derived from the 2-bromopyridinyl-substituted methylenecyclohexane 4
and also the vinyl- and the allyl-cyclohexanols 5 and 6, undergo endo-selective cyclizations to give six-, seven- and
eight-membered-ring annulated pyridines 7, 11 and 12.
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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/772/1/JOURNAL_OF_THE_CHEMICAL_SOCIETY%2DPERKIN_TRANSACTIONS_1_(15)1769%2D1773;2002[81].pdf
Maiti, Sarbendu and Achari, Basudeb and Mukhopadhyay, Ranjan and Banerjee, Asish Kr (2002) Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring systems by endo-selective 2-pyridyl radical cyclizations. Journal of the Chemical Society -Perkin Transactions, 1 (15). pp. 1769-1773. |
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| Relation |
http://dx.doi.org/10.1039/b204436f
http://www.eprints.iicb.res.in/772/ |
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