Tetrahedron

Direct oxidative conversion of aldehydes and alcohols to 2-imidazolines and 2-oxazolines using molecular iodine

M Ishihara, H Togo

Index: Ishihara, Midori; Togo, Hideo Tetrahedron, 2007 , vol. 63, # 6 p. 1474 - 1480

Full Text: HTML

Citation Number: 115

Abstract

Aldehydes were converted to the corresponding 2-imidazolines and 2-oxazolines in good yields by the reaction with ethylenediamine and aminoethanol, respectively, using molecular iodine and potassium carbonate. Moreover, primary alcohols were directly converted to the corresponding 2-imidazolines and 2-oxazolines via aldehydes in one-pot manner with ethylenediamine and aminoethanol, respectively, using molecular iodine and potassium ...

Related Articles:

Desulfitative Carbon–Carbon Cross??Coupling of Thioamide Fragments with Boronic Acids

[Prokopcova, Hana; Kappe, C. Oliver Advanced Synthesis and Catalysis, 2007 , vol. 349, # 3 p. 448 - 452]

One-pot synthesis of imidazolines from aldehydes: detailed study about solvents and substrates

[Tetrahedron, , vol. 63, # 3 p. 638 - 643]

Facile preparation of 2-imidazolines from aldehydes with tert-butyl hypochlorite

[Synthesis, , # 13 p. 1939 - 1942]

Highly practical synthesis of nitriles and heterocycles from alcohols under mild conditions by aerobic double dehydrogenative catalysis

[Organic Letters, , vol. 15, # 8 p. 1850 - 1853]

Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade

[Journal of Organic Chemistry, , vol. 76, # 18 p. 7482 - 7490]

More Articles...