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P III -Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles
A P(NMe 2 ) 3 -mediated reductive intramolecular cyclopropanation is developed for the first time, which provides facile access to a wide variety of cyclopropane-fused heterocycles including chromanes, tetrahydroquinolines, lactones, and lactams. Catalytic hydrogenative ring-expansion of the cyclopr...
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Published in: | Chemical communications (Cambridge, England) England), 2020-09, Vol.56 (70), p.10251-10254 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A P(NMe
2
)
3
-mediated reductive intramolecular cyclopropanation is developed for the first time, which provides facile access to a wide variety of cyclopropane-fused heterocycles including chromanes, tetrahydroquinolines, lactones, and lactams. Catalytic hydrogenative ring-expansion of the cyclopropane-fused heterocycles is also elaborated, leading to various structurally important medium-sized heterocycles. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/D0CC04086J |