75376-97-5Relevant academic research and scientific papers
The bioinspired design of a reagent allows the functionalization of Cα-H of α,β-unsaturated carbonyl compounds via the Baylis-Hillman chemistry under ambient conditions
Singh, Palwinder,Kumar, Arun,Kaur, Sukhmeet,Kaur, Jagroop,Singh, Harpreet
supporting information, p. 2936 - 2939 (2016/02/20)
A rationally designed reagent capable of affecting alkylation at Cα of α,β-unsaturated carbonyl compounds is reported. The reaction proceeded at room temperature without any additives. The pH and H-bond formation during the reaction play a key role in the working of the reagent.
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 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
