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Asymmetric Metal-Templated Route to Amino Acids with 3-Spiropyrrolidine Oxindole Core via a 1,3-Dipolar Addition of Azomethine Ylides to a Chiral Dehydroalanine Ni(II) Complex-spiropyrrolidine oxindole skeletal with continuous tetrasubstituted carbon stereocenters by a 1,3-dipolar
Synthesis and properties of phosphabetaine structures: IV. 3-(triphenylphosphonio)propanoate in reactions with dipolar electrophilic reagents and dicyclohexylcarbodiimide, we studied under the assumption that they proceed by nucleophilic addition and 1,4-dipolar
1,3 Dipolar cycloaddition of C-benzoyl-N-phenylnitrone to esters of vinyl-, β-cyanovinyl, and allylphosphosphonic acids and of C,N-diphenylnitrone to an allylphosphonic acid ester-dimethylphosphonoixoxazolidines. Only the first isomer is obtained in the reaction in boiling benzene. 2. The 1,3 dipolar addition
1,3 Dipolar cycloaddition of C-benzoyl-N-phenylnitrone to esters of vinyl-, β-cyanovinyl, and allylphosphosphonic acids and of C,N-diphenylnitrone to an allylphosphonic acid ester-dimethylphosphonoixoxazolidines. Only the first isomer is obtained in the reaction in boiling benzene. 2. The 1,3 dipolar addition
[3+2] Cycloaddition of o-nitrophenyl azide to 3a,6-epoxyisoindoles in substituted 3a,6-epoxyisoindoles was performed. The 1,3-dipolar addition reaction proceeded stereoselectively
Synthesis and properties of phosphabetaine structures: IV. 3-(triphenylphosphonio)propanoate in reactions with dipolar electrophilic reagents and dicyclohexylcarbodiimide, we studied under the assumption that they proceed by nucleophilic addition and 1,4-dipolar
Synthesis of new enantiopure amino acids with a 3-spiropyrrolidine oxindole core via a selective three-component 1,3-dipolar addition three-component 1,3-dipolar addition
Solid state NMR analysis of the dipolar couplings within and between distant CF(3)-groups in a membrane-bound peptideSolid state NMR analysis of the dipolar couplings within and between distant CF(3)-groups in a
On the theory of the proton dipolar-correlation effect as a method for investigation of segmental displacement in polymer melts et al. J. Chem. Phys. 144, 241101 (2016)] based on the proton NMR dipolar-correlation effect allowing
On the theory of the proton dipolar-correlation effect as a method for investigation of segmental displacement in polymer melts et al. J. Chem. Phys. 144, 241101 (2016)] based on the proton NMR dipolar-correlation effect allowing
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