Tetrahedron

Silver ion induced reactions of α-haloimines

N De Kimpe, C Stevens

Index: De Kimpe, Norbert; Stevens, Christian Tetrahedron, 1990 , vol. 46, # 19 p. 6753 - 6770

Full Text: HTML

Citation Number: 8

Abstract

The silver ion induced reactions of α-haloimines are markedly different from similar reactions with the corresponding α-haloketones. The various reactions of α-haloimines, including α- alkoxylation 1, 2-dehydrohalogenation, rearrangement via a-alkoxyaziridines, Favorskii- rearrangement and Wagner Meerwein rearrangement, are compared and evaluated with silver-induced reactions of a-haloketones The silver ion assisted reactions of α-haloimines ...

Related Articles:

Electrooxidative cyclization of N-acylhydrazones of aldehydes and ketones to. DELTA. 3-1, 3, 4-oxadiazolines and 1, 3, 4-oxadiazoles

[Chiba, Toshiro; Okimoto, Mitsuhiro Journal of Organic Chemistry, 1992 , vol. 57, # 5 p. 1375 - 1379]

Air-Persistent Monomeric (Amino)(carboxy) Radicals Derived from Cyclic (Alkyl)(Amino) Carbenes

[Welle, Frank; Verevkin, Sergej P.; Keller, Manfred; Beckhaus, Hans-Dieter; Ruechardt, Christoph Chemische Berichte, 1994 , vol. 127, # 4 p. 697 - 710]

Substituent effects on rates of formation of methoxy-substituted carbonyl ylides from 2-aryl-2-methoxy-and 5-aryl-2-methoxy-Δ3-1, 3, 4-oxadiazolines

[Bekhazi, Michel; Smith, Peter J.; Warkentin, John Canadian Journal of Chemistry, 1984 , vol. 62, p. 1646 - 1652]

Simple Phase Transfer Catalytic Method for α-Methoxylation of Sterically Hindered Ketones

[Abele; Rubina; Shymanska; Lukevics Synthetic Communications, 1995 , vol. 25, # 9 p. 1371 - 1376]

Substituent effects on rates of formation of methoxy-substituted carbonyl ylides from 2-aryl-2-methoxy-and 5-aryl-2-methoxy-Δ3-1, 3, 4-oxadiazolines

[Bekhazi, Michel; Smith, Peter J.; Warkentin, John Canadian Journal of Chemistry, 1984 , vol. 62, p. 1646 - 1652]

More Articles...