Synthesis of 1,2-oxazaheterocycles containing an isoindolone moiety fromN-Hydroxyphthalimide
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference16 articles.
1. Synthesis of dibenz[c,e]azepine and benzo[e]thieno[c]azepine via, N-acyliminium ion cyclization
2. Synthesis of thienothiazocinoisoindolediones and thienothiazinoisoindolones from mercaptothiophenes and chloromethylphthalimide
3. Selective access to N-aryl or N-alkyl derivatives of isoindolo[2,1-b][2,4]benzo(or thieno)diazepines
4. A facile fused-dioxaza-ring synthesis from N-hydroxyphthalimide
5. Lithium aluminum hydride reduction products from heterocycles containing an isoindolone nucleus
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1. Electrochemical behavior of N -oxyphthalimides: Cascades initiating self-sustaining catalytic reductive N ―O bond cleavage;Journal of Physical Organic Chemistry;2017-08-02
2. Synthesis of α-oxygenated ketones and substituted catechols via the rearrangement of N-enoxy- and N-aryloxyphthalimides;Tetrahedron;2017-07
3. Efficient Preparation of Biologically Important 1,2-Amino Alcohols;Synthetic Communications;2012-11-08
4. A direct arylation-oxidation route to 3-arylisoindolinone inhibitors of MDM2-p53 interaction;Tetrahedron Letters;2011-09
5. Gas-phase pyrolysis of N-alkoxyphthalimides to functionally substituted aldehydes: kinetic and mechanistic study;Arkivoc;2010-07-29
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