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Dive into the research topics where Claudine Pascard-Billy is active.

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Featured researches published by Claudine Pascard-Billy.


Journal of The Chemical Society, Chemical Communications | 1977

18-Crown-6–potassium–ethyl acetoacetate enolate. X-Ray structure determination

Claude Riche; Claudine Pascard-Billy; Christian Cambillau; G. Bram

The crystal structure of the title compound shows that it forms a distinct molecule; K+ is co-ordinated to the six oxygen atoms of the crown and to the two oxygen atoms of the U shaped enolate.


Journal of The Chemical Society, Chemical Communications | 1976

X-Ray structure of the androsta-14,16-diene–maleic anhydride adduct

Jean-Claude Beloeil; Claudine Pascard-Billy; Thierry Prangé

The Diels-Alder reaction of the reactive androsta-14,16-diene with maleic anhydride has been shown to be a β-attack of the D ring of the molecule.


Journal of The Chemical Society, Chemical Communications | 1975

X-Ray structure of mascaroside, a new bitter glycoside from coffee beans

Arnaud Ducruix; Claudine Pascard-Billy; Michèle Hamonniere; Jacques Poisson

The structure of mascaroside, a bitter glycoside from Coffea vianneyi, has been shown by spectroscopic methods and X-ray analysis to be a diterpene, of the (–)-kaurene type with a β-glucose unit attached to C-17.


Journal of The Chemical Society, Chemical Communications | 1975

Crystal and molecular structure of emericid: a new polyether antibiotic

Claude Riche; Claudine Pascard-Billy

The molecular structure of the antibiotic emericid has been established from the crystal structure of its silver salt.


Journal of The Chemical Society, Chemical Communications | 1974

Synthesis and stereochemical correlation of acyclic sugar nucleoside analogues: X-ray crystal structure of (1R)-2,3,4,5-tetra-O-acetyl-1-S-ethyl-1-(1,6-dihydro-6-thioxopurin-9-yl)-1-thio-D-arabinitol

David C. Baker; Arnaud Ducruix; Derek Horton; Claudine Pascard-Billy

A crystal structure determination has been used to establish the absolute stereochemistry of a mixed acetal derivative, a nucleoside analogue (1) having purine-6-thione (‘6-mercaptopurine’) attached to an acyclic D-arabinose derivative.


Journal of The Chemical Society, Chemical Communications | 1974

Synthesis and X-ray crystallographic studies of dithiepan derivatives of carbohydrates

Alice Gateau-Olesker; S.D. Gero; Claudine Pascard-Billy; Claude Riche; Anne-Marie Sepulchre; Georges Vass; Neil A. Hughes

Nucleophilic addition of 2-lithio-2-methyl-1,3-dithian to the dialdehyde (2) gives the two diastereo-isomers (3) and (7) was transformed into a new class of carbohydrate dithiepan derivatives (11)–(13).


Journal of The Chemical Society, Chemical Communications | 1973

X-Ray crystal and molecular structure of pollinastanol acetate, a 9,19-cyclopropane steroid

Arnaud Ducruix; Claudine Pascard-Billy; Michel Devys; Michel Barbier; Edgar Lederer

The structure of pollinastanol acetate has been elucidated by direct method X-ray crystal structure analysis; it is the acetate of 14α-methyl-9β,19-cyclo-5α-cholestan-3β-ol (I).


Tetrahedron Letters | 1974

Structure cristalline et moleculaire de la phomenone, phytotoxine produite par le champignon Phoma exigua var. non oxydabilis.

Claude Riche; Claudine Pascard-Billy; Michel Devys; A. Gaudemer; Michel Barbier; Jean-François Bousquet


Tetrahedron | 1978

Enolates de l'acetylacetate d'ethyle. Structure et reactivite du sel de potassium en presence d'ether couronne et de cryptand

C. Cambillau; G. Bram; J. Corset; Claude Riche; Claudine Pascard-Billy


Carbohydrate Research | 1973

Conformation of 2-S-ethyl-2-thio-D-mannose diethyl dithioacetal in the crystalline state and in solution

Arnaud Ducruix; Claudine Pascard-Billy; Derek Horton; Joseph D. Wander

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Arnaud Ducruix

Institut de Chimie des Substances Naturelles

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Claude Riche

Institut de Chimie des Substances Naturelles

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Michel Barbier

Institut de Chimie des Substances Naturelles

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Anne-Marie Sepulchre

Institut de Chimie des Substances Naturelles

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G. Bram

University of Paris-Sud

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Georges Vass

Institut de Chimie des Substances Naturelles

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Michel Devys

Institut de Chimie des Substances Naturelles

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A. Gaudemer

University of Paris-Sud

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