B. D'hooge scite author profile

stereochemistry stereochemistry (general, optical resolution) O 0030 -043Stereoisomerism in the Adducts of Appel's Salt with Activated Methylenes.-Reaction of Appel's salt (I) with activated methylene compounds provides adducts, of which some of them display an interesting equilibrium between two stereoisomers, e.g. (V) and (VI), which have either a S···O or a S···N interaction. -(D'HOOGE, B.; DEHAEN, W.; Bull. Soc.

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1,2,3Thiadiazoles as a Convenient Source for the Study of Molecular Rearrangements, Single Bond/No Bond Resonance and Dendrimer Synthesis

L'abbé

D'hooge

Dehaen

1997

Molecules

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B. D'hooge

Nucleophilic Intramolecular Cyclization Reactions of Alkynechalcogenolates

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ChemInform Abstract: Stereoisomerism in the Adducts of Appel′s Salt with Activated Methylenes.

1,2,3Thiadiazoles as a Convenient Source for the Study of Molecular Rearrangements, Single Bond/No Bond Resonance and Dendrimer Synthesis

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B. D'hooge

Nucleophilic Intramolecular Cyclization Reactions of Alkynechalcogenolates

Unusual behaviour of 4,5-dichloro-1,2,3-dithiazolium chloride (Appel's salt) with 5-aminopyrazoles: a synthetic method of 1H-pyrazolo[3,4-d]thiazoles

A general synthesis of benzofuran-2-thiolates via intramolecular addition of phenolates to alkynethiolates

ChemInform Abstract: Stereoisomerism in the Adducts of Appel′s Salt with Activated Methylenes.

1,2,3Thiadiazoles as a Convenient Source for the Study of Molecular Rearrangements, Single Bond/No Bond Resonance and Dendrimer Synthesis

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1,2,3Thiadiazoles as a Convenient Source for the Study of Molecular Rearrangements, Single Bond/No Bond Resonance and Dendrimer Synthesis