An MEDT Study of the Reaction Mechanism and Selectivity of the Hetero-Diels-Alder Reaction Between 3-Methylene-2,4-Chromandione and Methyl Vinyl Ether. [PDF]
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Three-component diels-alder reaction through palladium carbene migratory insertion enabled dearomative C(sp3)-H bond activation. [PDF]
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Sustainable tandem acylation/Diels-Alder reaction toward versatile tricyclic epoxyisoindole-7-carboxylic acids in renewable green solvents. [PDF]
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Kinetic Study of the Diels-Alder Reaction between Maleimide and Furan-Containing Polystyrene Using Infrared Spectroscopy. [PDF]
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Inverse Electron Demand Diels-Alder Reaction on M<sub>3</sub>N@C<sub>80</sub> (M=Lu, Sc): Reactivity and Reversibility Enable Chemical Separation of Metallofullerenes. [PDF]
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Intramolecular Diels–Alder reactions of N-substituted oxazolones
Chemical Communications, 2002The first intramolecular Diels-Alder reactions of simple trienes featuring an N-substituted oxazolone as the dienophilic component have been investigated and are reported herein.
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In the preparation of rigid and annulated tricyclic bis(α-amino acid) derivatives the key construction was effected by a Ru(II)-catalyzed RCM cascade reaction of gem-dienynes. The substrates were available by stepwise and stereocontrolled alkynylations and alkenylations of (2R)-2,5-dihydro-2-isopropyl-3,6-dimethoxypyrazine.
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AbstractFor Abstract see ChemInform Abstract in Full Text.
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