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
Hauptverfasser: Efremova, M. M., Kostikov, R. R., Larina, A. G., Molchanov, A. P.
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container_issue 2
container_start_page 246
container_title Russian journal of organic chemistry
container_volume 53
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
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source SpringerNature Journals
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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