80780-67-2Relevant academic research and scientific papers
Effect of chalcogenyl substituent on the course of allyl rearrangement at chalcogenation of 1,3-dichloropropene
Levanova,Nikonova,Grabel’nykh,Russavskaya,Albanov,Rozentsveig,Korchevin
, p. 615 - 623 (2016/07/06)
Formation of 1,3-dichalcogenylpropene at the treatment of 1,3-dichloropropene with organic dichalcogenides in a redox system hydrazine hydrate–KOH is governed by the possibility of an allyl rearrangement. In the presence of bases this rearrangement proceeds via carbanion partially stabilized by the chalcogenyl substituent. The effectivity of the stabilization and consequently the probability of the rearrangement varies in the series of substituents PhS > BnS > PhSe. In the stage of the direct nucleophilic substitution of chlorine the anion PhSe?possesses the highest activity.
Syntheses d'alcools allyliques et alleniques fonctionnels a partir de composes carbonyles α-phenylselenies
Lerouge, Patrice,Paulmier, Claude
, p. 1225 - 1229 (2007/10/02)
The functionalized allylic selenides 6, 7, 8, 10 and 11 were prepared from phenylselenoaldehydes and ketones 1, and phenylselenopyruvates 2 using the Wittig or the Horner reaction. 2,3-Sigmatropic rearrangement of the corresponding selenoxides leads to the functional allylic alcohols 15, 16 and 17 and to the conjugated enals 18, 19 and 20.A method for the conversion of an aldehyde into the enal with an additional carbon is described.The functional 3-phenylselenobutadienes 23, 24 and 25 were also obtained from α-phenylselenoenals 21 in the same manner.An oxidation-rearrangement reaction appears to be a convenient way to prepare the functional or substitued allenic alcohols 26 and 28.The ethyl 2-hydroxy pent-3,4-dienoate 26c has been cyclized by benzeneselenenyl bromide into the ethyl 2,5-dihydrofurancarboxylate 29.
PROPRIETES DES α-PHENYLSELENOALDEHYDES REACTIONS DE WITTIG CONDUISANT A DES α-HYDROXYESTERS ET CETONES β,γ-ETHYLENIQUES ET A DES ALDEHYDES α,β-ETHYLENIQUES
Lerouge, Patrice,Paulmier, Claude
, p. 1983 - 1986 (2007/10/02)
Wittig and Wittig-Horner reactions with α-phenylselenoaldehydes lead to allylic selenides.The corresponding selenoxides undergo 2,3-sigmatropic rearrangement providing a route to α-hydroxy β,γ-ethylenic esters and ketones in good yields.In a some way, we prepare, also enals with an additional carbon.
Selenium-Stabilized Carbanions. Synthesis of Enals and Silyl Enones Using 1,3-Bis(phenylseleno)propene
Reich, Hans J.,Clark, Mark C.,Willis, W.W.
, p. 1618 - 1623 (2007/10/02)
The utility of 1,3-bis(phenylseleno)propene (4) as a propenone synthon having n3 (1) or n1 and n3 (3) reactivity has been examined.Deprotonation of 4 with lithium diisopropylamine in THF at -78 deg C proceeds to give a lit
