38846-14-9Relevant academic research and scientific papers
Base Catalysed Rearrangements involving Ylide Intermediates. Part 6. The Rearrangements of Diallyl- and Allylpropynyl-ammonium Cations in Protic Media
Laird, Trevor,Ollis, W. David,Sutherland, Ian O.
, p. 1477 - 1486 (2007/10/02)
The base catalysed rearrangements of the cations (1d-j) in aqueous solution yield the isomeric cations (15) or the aldehydes (10) and (11), or mixtures of (15), (10), and (11).This contrasts dramatically with the transformations observed for the cations (1) in aprotic solvents.The cations (15) undergo Hofmann elimination to the naphthalenic amines (12) or (13) and (14).The methiodide of amine (13g) shows a novel consequence of restricted rotation.The n.m.r. spectrum of the methiodide shows that the two protons of the methylene group are diastereotopic.
Base-catalysed rearrangement of allyl-propynyl ammonium cations and a novel synthetic route to substituted biphenyls
Jemison,Laird,Ollis
, p. 556 - 557 (2007/10/06)
Base-catalysed rearrangement of the salts (I) in aprotic media gives the amines (II) and (III); the amines (II) on heating yield the biphenyl derivatives (V).
Base-catalysed rearrangement of allyl-propynyl ammonium cations in protic media
Laird,Ollis
, p. 557 - 559 (2007/10/05)
The base-catalysed rearrangement of the allylpropynyl ammonium cations (I) in aqueous solution yields either the isomeric cations (II) or the aldehydes (III) and (IV), or mixtures of (II), (III), and (IV); this result contrasts dramatically with the trans
