Stefan Jopp

Affiliations: 
2016-2018 Chemistry University of Rostock, Rostock, Mecklenburg-Vorpommern, Germany 
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"Stefan Jopp"
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Lehmann P, Jopp S. (2023) Excellence in Acrylation - Scope and Limitation of Glucosyl Imidazolium-coated Novozym 435 Catalyzed (Meth)acryl Ester Synthesis. Chemistry, An Asian Journal. e202300918
Tka N, Ayed MAH, Braiek MB, et al. (2021) 2,4-Bis(arylethynyl)-9-chloro-5,6,7,8-tetrahydroacridines: synthesis and photophysical properties. Beilstein Journal of Organic Chemistry. 17: 1629-1640
Longwitz L, Jopp S, Werner T. (2019) Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. The Journal of Organic Chemistry. 84: 7863-7870
Langer P, Jopp S, Ehlers P, et al. (2019) Site-Selective Synthesis of 3,17-Diaryl-1,3,5,16-estratetraenes Synlett. 30: 600-604
Jopp S, Molenda R, Seiler ERD, et al. (2019) Total Synthesis of Dabigatran Revisited; Synthesis of Amidine‐Tosylated Dabigatran Chemistryselect. 4: 13802-13805
Jopp S, Liesegang M, Ehlers P, et al. (2018) Synthesis of novel 16-E-(arylidene)-3-methoxy-α-estrones via a palladium catalysed Suzuki-Miyaura reaction Tetrahedron Letters. 59: 26-28
Jopp S, Wallaschkowski T, Ehlers P, et al. (2018) Chemoselective Suzuki-Miyaura reactions of 4-bromo-3- O -triflyl-estrone. Synthesis and atropisomerism of arylated estrones Tetrahedron. 74: 2825-2836
Langer P, Jopp S, Liesegang M, et al. (2017) Palladium-Catalysed Sonogashira Reactions of 16-(Hydroxymethylidene)-3-methoxy-α-estrone Synlett. 28: 2647-2649
Riebe S, Jopp S, Ehlers P, et al. (2017) Synthesis of 16- E -([aryl]idene)-3-methoxy-estrones by a palladium catalysed Mizoroki-Heck reaction Tetrahedron Letters. 58: 2801-2803
Ehlers P, Petrosyan A, Baumgard J, et al. (2013) ChemInform Abstract: Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids. Cheminform. 44: no-no
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