J
Joseph Schoepfer
Researcher at University of Neuchâtel
Publications - 3
Citations - 21
Joseph Schoepfer is an academic researcher from University of Neuchâtel. The author has contributed to research in topics: Thiocyanic acid & Ene reaction. The author has an hindex of 2, co-authored 3 publications receiving 21 citations.
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Lewis-acid catalysed tandem reaction Diels–Alder–[3,3] sigmatropic shift between buta-1,3-dienyl thiocyanic acid ester and acryloyl chloride: application in the synthesis of 2-azabicyclo[2.2.2]oct-5-ene derivatives
TL;DR: In this paper, a 1,3-dienyl thiocyanic acid ester reacts with acryloyl chloride in presence of Lewis acid catalysts to produce directly the rearranged product of type 3b via a combination of a Diels-Alder reaction with a [3,3] sigmatropic shift; the 1,4-substituted cyclohexene is easily transformed into the 2-azabicyclo[2.2] oct-5-ene derivative 6b, which has been used as precursor for the
Journal ArticleDOI
The Stereochemistry of the 1,4-Elimination of Thiocyanic Acid from Hex-3-ene-2,5-diyl Dithiocyanates
TL;DR: The elimination of thiocyanic acid from the stereoisomers of the hex-3-ene-2,5-diyl dithIocyanates, 4a, 4b, 6a and 6b, was studied in this article.
Journal ArticleDOI
The Stereochemistry of the 1,4‐Elimination of Thiocyanic Acid from Hex‐ 3‐ene‐2,5‐diyl Dithiocyanates.
TL;DR: The elimination of thiocyanic acid from the stereoisomers of the hex-3-ene-2,5-diyl dithIocyanates, 4a, 4b, 6a and 6b, was studied in this article.