Tetrahedron

Studies on cycloaddition reactions of 1, 3-diphenyl-2-azaallyl lithium and ethyl (benzylideneamino) acetate anion with α-oxoketene dithioacetals

MP Balu, H Ila, H Junjappa

Index: Balu, Maliakel P.; Ila, Hiriyakkanavar; Junjappa, Hiriyakkanavar Tetrahedron, 1990 , vol. 46, # 19 p. 6771 - 6782

Full Text: HTML

Citation Number: 10

Abstract

The α-oxoketene dithioacetals undergo anionic [1, 3] cycloaddition with l, 3-diphenyl-2- azaallyllithium to give either pyrroles or spiropyrrolines with two exceptions. Lithium bromide/triethylamine induced cycloaddition of ethyl (benzylideneamino) acetate (7) with acyclic ct-oxoketene dithioacetals afforded either pyrrolidine, pyrrole or the corresponding 3- benzylideneamino-pyran-2-one derivatives depending on the reaction conditions and the ...

Related Articles:

Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers

[Jiang, Yaojia; Chan, Wei Chuen; Park, Cheol-Min Journal of the American Chemical Society, 2012 , vol. 134, # 9 p. 4104 - 4107]

Organische Synthesen mit Übergangsmetall-Komplexen XLV. 3-Hydroxypyridine, 1H-Pyrrole und 2-Hydroxypyrrol-Derivate aus einem Aminocarben-Chromkomplex …

[Aumann, Rudolf; Heinen, Heinrich Journal of Organometallic Chemistry, 1990 , vol. 389, # 1 p. C1 - C6]

More Articles...