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Concertedness of 1,3-dipolar cycloadditions
Journal of Chemical Education, 1984The 1,3-dipolar cycloaddition is the union of a 1,3-dipole with a multiple bond system (a dipolarophile) to form a five-membered ring; the process is regarded as one of the most general methods for the synthesis of five-membered heterocycles.
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Intramolecular 1,3‐Dipolar Cycloaddition Reactions
Angewandte Chemie International Edition in English, 1976AbstractThe intramolecular 1,3‐dipolar cycloaddition reaction of suitably functionalized 1,3‐dipoles represents a general scheme for the synthesis of novel fused ring heterocycles. Such reactions of a number of 1,3‐dipoles are summarized and the general outline and potential analogies for these reactions noted. While the immediate aim of this review is
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
exaly
1,3-dipolar cycloadditions with porphyrins
2009The objective of this work is to use 1,3-dipolar cycloadditions to synthesize novel aromatic compounds based on meso-phenyl substituted porphyrins. These compounds are potential photosensitizers for use in photodynamic therapy. Tetraphenylporphyrins with a variety of substituents were reacted with selected 1,3-dipoles.
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Asymmetric 1,3-Dipolar Cycloaddition Reactions
Chemical Reviews, 1998Kurt V., Gothelf, Karl Anker, Jørgensen
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