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Dive into the research topics where Pierre Barbier is active.

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Featured researches published by Pierre Barbier.


Contact Dermatitis | 1985

Enantiospecificity in allergic contact dermatitis A review and new results in Frullania‐sensitive patients

Claude Benezra; Jean-Luc Stampf; Pierre Barbier; Geirges Ducombs

Allergic contact dermatitis is essentially enantiospceific: sensitization to one enantiomer generally does not imply elicitation to the mirror‐image allergens. Examples from patients allergic to Frullania. and from the literature (usnic acids. 4‐methoxydalbergioes, γ‐methyl‐α‐methylene‐γ‐butyrolactones, frullanolides) are discussed.


Archives of Dermatological Research | 1981

Allergic contact dermatitis to various salols (phenyl salicylates)

Bernard Marchand; Pierre Barbier; Georges Ducombs; Jean Foussereau; Pierre Martin; Claude Benezra

SummaryPatients sensitive to phenyl salicylate (salol) were patch-tested to several aryl salicylates. The most powerful derivative was p-nitrophenyl salicylate (compound 5). This can be explained by an unusually good interaction with protein (nucleophilic substitution on the carboxyl carbon). All these results were confirmed by experimental sensitization of guinea pigs to salol and cross-reaction to substituted salols. The results are in line with current theory of allergic contact dermatitis, i.e., an in vivo formation of a hapten-protein conjugate.


Tetrahedron Letters | 1982

A one-step synthesis of 2-phenylthio-2-buten-4-olides.

Pierre Barbier; Claude Benezra

Abstract The title compounds are prepared by the reaction of an α-acetoxy aldehyde with ethyl phenylthioacetate.


Journal of Organic Chemistry | 1988

Synthesis of tetrahydrolipstatin and tetrahydroesterastin, compounds with a .beta.-lactone moiety. Stereoselective hydrogenation of a .beta.-keto .delta.-lactone and conversion of the .delta.-lactone into a .beta.-lactone

Pierre Barbier; Fernand Schneider


Journal of Medicinal Chemistry | 1986

Allergenic alpha-methylene-gamma-butyrolactones. Study of the capacity of beta-acetoxy- and beta-hydroxy-alpha-methylene-gamma-butyrolactones to induce allergic contact dermatitis in guinea pigs.

Pierre Barbier; Claude Benezra


Journal of Medicinal Chemistry | 1982

Allergenic alpha-methylene-gamma-butyrolactones. Stereospecific syntheses of (+)- and (-)-gamma-methyl-alpha-methylene-gamma-butyrolactones. A study of the specificity of (+) and (-) enantiomers in inducing allergic contact dermatitis.

Pierre Barbier; Claude Benezra


Archive | 1996

Dermatological use of vitamin d derivatives

Pierre Barbier; Marc Muller; Josef Stadlwieser


Archive | 2004

Retiferol derivatives and their use in the treatment of skin diseases or conditions associated with photodamage

Pierre Barbier; Franz Bauer; Peter Mohr; Marc Muller; Wolfgang Pirson


Archive | 1998

Novel vitamin d3 amide derivatives

Pierre Barbier; Franz Bauer; Peter Mohr; Marc Muller; Wolfgang Pirson


Tetrahedron Letters | 1982

A short stereoselective synthesis of (±)-litsenolides C1 and C2.

Pierre Barbier; Claude Benezra

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Claude Benezra

Centre national de la recherche scientifique

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