Synthesis of (±)-Bisavenanthramide B-6 by an Anionic Anhydride Mannich Reaction
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چکیده
منابع مشابه
Synthesis of Polyamide 6 by Anionic Polymerization of ε-Caprolactam in an Internal Mixer: Effect of Polymerization Reaction Time
The main objective of the present work was to synthesis polyamide 6 through anionic polymerization of ε-caprolactam in an internal mixer. The reaction time and the rheological properties of samples during the polymerization were studied. The samples were characterized by Thermo Gravimetry Analysis (TGA), Differential Scanning Calorimeter (DSC) and FT-IR spectrometer. The melt flow behavior and ...
متن کاملsynthesis of polyamide 6 by anionic polymerization of ε-caprolactam in an internal mixer: effect of polymerization reaction time
the main objective of the present work was to synthesis polyamide 6 through anionic polymerization of ε-caprolactam in an internal mixer. the reaction time and the rheological properties of samples during the polymerization were studied. the samples were characterized by thermo gravimetry analysis (tga), differential scanning calorimeter (dsc) and ft-ir spectrometer. the melt flow behavior and ...
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A complement to the classic three-component Mannich reaction, the redox-Mannich reaction, utilizes the same starting materials but incorporates an isomerization step that enables the facile preparation of ring-substituted β-amino ketones. Reactions occur under relatively mild conditions and are facilitated by benzoic acid.
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An NHC-catalyzed regio- and stereoselective Mannich/lactamization domino reaction of N-(benzothiazolyl)imines with α-chloroaldehydes has been developed. This new protocol provides a facile approach for the asymmetric synthesis of benzothiazolo-pyrimidinones and a pyrrolo[1,2-a]indolone in moderate to good yields (34-78%) and excellent stereoselectivities (87-99% ee, up to >20 : 1 d.r.).
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A new chemoselective reductive nitro-Mannich cyclization reaction sequence of nitroalkyl-tethered lactams has been developed. Relying on the rapid and chemoselective iridium(I)-catalyzed reduction of lactams to the corresponding enamine, subsequent nitro-Mannich cyclization of tethered nitroalkyl functionality provides direct access to important alkaloid natural-product-like structures in yield...
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ژورنال
عنوان ژورنال: Organic Letters
سال: 2016
ISSN: 1523-7060,1523-7052
DOI: 10.1021/acs.orglett.6b00413