Sequential 1,3‐Dipolar Cycloaddition of Nitrones to β‐(2‐Aminophenyl) α,β‐Ynones and Cyclocondensation: A New Entry to the Isoxazolino[4,5‐ c ]quinoline Ring | Zendy

Abbiati Giorgio | Zendy; Arcadi Antonio | Zendy; Marinelli Fabio | Zendy; Rossi Elisabetta | Zendy; Verdecchia Mirella | Zendy

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Sequential 1,3‐Dipolar Cycloaddition of Nitrones to β‐(2‐Aminophenyl) α,β‐Ynones and Cyclocondensation: A New Entry to the Isoxazolino[4,5‐ c ]quinoline Ring

Author(s) -

Abbiati Giorgio,

Arcadi Antonio,

Marinelli Fabio,

Rossi Elisabetta,

Verdecchia Mirella

Publication year - 2009

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200800994

Subject(s) - chemistry , quinoline , annulation , cycloaddition , ring (chemistry) , 1,3 dipolar cycloaddition , medicinal chemistry , combinatorial chemistry , organic chemistry , stereochemistry , catalysis

The reaction of β‐(2‐aminophenyl) α,β‐ynones with N ‐methyl nitrones provides a simple and efficient entry to the isoxazolino[4,5‐ c ]quinoline ring system through a sequential 1,3‐dipolar cycloaddition/annulation process. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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