Stereoselective synthesis of (E,Z)-3,4-dialkylidene-N-phenylpyrrolidine-2,5-diones starting from Morita–Baylis–Hillman carbonates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference47 articles.
1. Regioselective synthesis of 2,4,5-trisubstituted thiophenes from Morita–Baylis–Hillman adduct-derived phosphorous ylides and isothiocyanates
2. One-pot, three-component synthesis of arylidenesuccinates and related compounds
3. A Practical Route to Substituted 7-Aminoindoles from Pyrrole-3-carboxaldehydes
4. Dihydro-3-(triphenylphosphoranylidene)-2,5-thiophendione: a convenient synthon for the preparation of substituted 1,4-thiazepin-5-ones and piperidinones via the intermediacy of thioacids
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3. Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework;Tetrahedron;2018-05
4. Organocatalytic Synthesis of 4-Aryl-1,2,3,4-tetrahydropyridines from Morita-Baylis-Hillman Carbonates through a One-Pot Three-Component Cyclization;The Journal of Organic Chemistry;2018-01-10
5. Synthesis of dispirocyclohexadiene bisoxindole from Morita-Baylis-Hillman carbonate of isatin;Tetrahedron Letters;2017-08
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