Construction of alpha -amido-indanones viaformal allenamide hydroacylation-Nazarov cyclization
A two-step modular synthesis of an alpha -hydroxycyclopentenone and alpha -amido-indanones has been developed based on the Nazarov cyclization of 2-amido-1,4-pentadien-3-ones, readily accessed viaformal hydroacylation of allenamides.
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2012-08, Vol.48 (73), p.9186-9188 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Wu, Yen-Ku Niu, Tianmin West, F G |
description | A two-step modular synthesis of an alpha -hydroxycyclopentenone and alpha -amido-indanones has been developed based on the Nazarov cyclization of 2-amido-1,4-pentadien-3-ones, readily accessed viaformal hydroacylation of allenamides. |
doi_str_mv | 10.1039/c2cc34644c |
format | Article |
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ispartof | Chemical communications (Cambridge, England), 2012-08, Vol.48 (73), p.9186-9188 |
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language | eng |
recordid | cdi_proquest_miscellaneous_1283709234 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Construction Modular Synthesis |
title | Construction of alpha -amido-indanones viaformal allenamide hydroacylation-Nazarov cyclization |
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