Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through ?(????)-O Bond Formation
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ID: 10993
2011
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Abstract
1,4-benzoxathiine moieties can be synthesized by domino SN2 ring opening of epoxide with o-halothiophenols followed by the copper(I)-BINOL catalyzed Ullmann-type coupling cyclization (intramolecular C(aryl)-O bond formation) with moderate to good yields.
| Reference Key |
chiranjeevi2011copperibinolorganic
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| Authors | Korupalli, Chiranjeevi;Dandapat, Arpan;Prasad, D. J. C.;Sekar, Govindasamy;Korupalli, Chiranjeevi;Dandapat, Arpan;Prasad, D. J. C.;Sekar, Govindasamy; |
| Journal | organic chemistry international |
| Year | 2011 |
| DOI |
10.1155/2011/980765
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| URL | |
| Keywords | Keywords not found |
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