The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations. [PDF]
Seidel D.
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Catalytic [6 + 3] cycloaddition for the synthesis of medium-sized ring systems: a critical review. [PDF]
Archna +4 more
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Metal-free α-amination of secondary amines: computational and experimental evidence for azaquinone methide and azomethine ylide intermediates. [PDF]
Dieckmann A +5 more
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Synthesis of heterocycles based on azomethine ylides from α-amino acids (or amines) and carbonyl compounds. [PDF]
Berezhnaya EV +3 more
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Recent advances of azomethine ylides for the synthesis of natural and synthetic bioactive pyrrolidines and spiropyrrolidines. [PDF]
Paira P +4 more
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Advances in the biomimetic and Maillard route synthesis and regulation of pyrazine flavour compounds. [PDF]
Wang B, Zhao Y, Zhao L, Zhu W, Ren J.
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The Chemistry of Azomethine Ylides Developed in the Institute
The research on azomethine ylide 1,3-dipoles, developed in the last five years in the Institute of Advanced Material Study, Kyushu University, is briefly reviewed.
カネマサ, シュウジ +2 more
core
Cycloaddition Reactions of Sulfo-Biginelli Derived Thiadiazines. [PDF]
Hill CL, Sambor M, Yang A, Wipf P.
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