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Showing papers in "Synthesis in 1986"


Journal ArticleDOI
TL;DR: In this article, the authors discuss applications catalytiques du Nafion H and de ses derives modifies en synthese organique. And they present a survey of applications of catalytique.
Abstract: Revue des applications catalytiques du Nafion H et de ses derives modifies en synthese organique

250 citations


Journal ArticleDOI
TL;DR: In this paper, the same epoxydation is fait avec l'hydroperoxyde de t-butyle en presence of propanolate-2 de titane IV avec le tartrate de dialkyle chiral, and exemples de synthese de composes naturels enantiomeriquement purs par l'intermediaire d'epoxydes obtenus par cet.
Abstract: Cette epoxydation se fait avec l'hydroperoxyde de t-butyle en presence de propanolate-2 de titane IV avec le tartrate de dialkyle chiral; exemples de synthese de composes naturels enantiomeriquement purs par l'intermediaire d'epoxydes obtenus par cette reaction asymetrique

196 citations












Journal ArticleDOI
TL;DR: In this article, a useful method for the preparations of 1-alkenes from terminal allylic carbonates and acetates by the palladium-catalyzed reaction with formates is described.
Abstract: A useful method for the preparations of 1-alkenes from terminal allylic carbonates and acetates by the palladium-catalyzed reaction with formates is described. Formic acid-triethylamine is a suitable reductant. As catalyst, Pd2(dba)3CHCl3-P(n-Bu)3, gave the best results. 0.05 0.2mol% being sufficient (turnover 500 2000). Using this method, various 1-alkenes were prepared in good yields with high selectivity.

Journal ArticleDOI
TL;DR: In this paper, the methodes de clivage reducteur de groupes nitro aliphatiques utilisant le tributylstannane and leurs applications in synthese organique are discussed.
Abstract: Revue des methodes de clivage reducteur de groupes nitro aliphatiques utilisant le tributylstannane et leurs applications en synthese organique

Journal ArticleDOI
TL;DR: Synthese respectivement a partir de l'orthoacetate de triethyle et de dialkylacetals of l'acetone et acetophenone as mentioned in this paper.
Abstract: Synthese respectivement a partir de l'orthoacetate de triethyle et de dialkylacetals de l'acetone et acetophenone


Journal ArticleDOI
TL;DR: The use of Dimethyl Carbonate as a Methylating Agent under Phase Transfer-Catalysed Conditions Dimethyl carbonate (as well as diethyl, diallyl, dibenzyl carbonate and ethane-1, 2-diyl carbonates) is a versatile, cheap, and safer reagent for the methylation of a variety of organic substrates as discussed by the authors.
Abstract: Use of Dimethyl Carbonate as a Methylating Agent under Phase Transfer-Catalysed Conditions Dimethyl carbonate (as well as diethyl, diallyl, dibenzyl carbonate and ethane-1, 2-diyl carbonate) in the presence of potassium carbonate and 18-crown-6 (or Aliqual 336) is a versatile, cheap, and safer reagent for the methylation of a variety of organic substrates.


Journal ArticleDOI
TL;DR: In this article, a basique basique d'alcoxy-and phenoxy-4 trihalogeno-1, 1, 1 butene-3ones-2 en les acides acryliques du titre; de la meme facon, synthese des heterocycles du titres a partir des trihalogensoacetyl-5 dihydro-3,4 pyrannes and trihalogeneoacetymethyl-4 dihydroid-2,3 furannes.
Abstract: Hydrolyse basique d'alcoxy- et phenoxy-4 trihalogeno-1,1,1 butene-3ones-2 en les acides acryliques du titre; de la meme facon, synthese des heterocycles du titre a partir des trihalogenoacetyl-5 dihydro-3,4 pyrannes et trihalogenoacetyl-4 dihydro-2,3 furannes






Journal ArticleDOI
TL;DR: In this paper, the reaction of carbonates with amines primaires and secondaires and α-aminoacides was studied in the setting of carbonate carbonates and amines.
Abstract: Reaction des (alkyl chloro-1 ethyl) carbonates avec des amines primaires et secondaires et avec des α-aminoacides





Journal ArticleDOI
TL;DR: Conversion par reaction avec des amides d'acides sulfoformimidiques as mentioned in this paper, a.k.a., guanidino-2 alcanoiques
Abstract: Conversion par reaction avec des amides d'acides sulfoformimidiques. Obtention des acides guanidino-2 alcanoiques