23718-97-0Relevant articles and documents
Synthesis of β-lactams via cycloaddition of hydrazones with phenoxyketene
Sharma,Pandhi
, p. 2196 - 2200 (2007/10/02)
Phenoxyketene is capable of annelating the disubstituted hydrazones to afford stereoselectivity cis-monocyclic β-lactams with a 1-amino functionality. The ease of cycloaddition is governed by substitutents on the azomethine carbon as well as on the hydraz
Rearrangement of Arylhydrazones of α,β-Unsaturated Carbonyl Compounds in Polyphosphoric Acid. 6
Fusco, Raffaello,Sannicolo, Franco
, p. 4374 - 4378 (2007/10/02)
The reactions of a series of N-methyl-N-arylhydrazones of α,β-unsaturated carbonyl compounds 1 with hot polyphosphoric acid are described.Three main courses were observed, depending on the structure of the carbonyl portion of the substrate.Unsaturated α-oxo ester hydrazones (1a-c) rearranged to give substituted 3--2-oxo-3-butenoic acid esters (2a-c); the reaction mechanism strictly resembles the initial steps of the Fischer indole synthesis.Unsaturated aldehyde hydrazones alternatively gave either the di-3-indolylmethane derivatives (3a,b) or the amino nitriles (4a-c).The first process develops through intermediates structurally similar to 2; the latter was demonstrated to be exclusively intramolecular.
