Regio- and stereoselective (3 + 2)-cycloaddition of nitrile oxides and nitrones to N-vinylindole
1,3-Dipolar cycloaddition of nitrile oxides and nitrones to N -vinylindole proceeds regioselectively at the exocyclic multiple bond to form 5-indolyl-substituted isoxazolines and isoxazolidines in good yields.
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Veröffentlicht in: | Russian journal of organic chemistry 2017-02, Vol.53 (2), p.246-250 |
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container_title | Russian journal of organic chemistry |
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creator | Efremova, M. M. Kostikov, R. R. Larina, A. G. Molchanov, A. P. |
description | 1,3-Dipolar cycloaddition of nitrile oxides and nitrones to
N
-vinylindole proceeds regioselectively at the exocyclic multiple bond to form 5-indolyl-substituted isoxazolines and isoxazolidines in good yields. |
doi_str_mv | 10.1134/S107042801702018X |
format | Article |
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N
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subjects | Chemistry Chemistry and Materials Science Cycloaddition Isoxazolidines Organic Chemistry Stereoselectivity |
title | Regio- and stereoselective (3 + 2)-cycloaddition of nitrile oxides and nitrones to N-vinylindole |
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