Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Melanie Denißen"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2340-2351 (2017)
In situ activation of 3-arylpropiolic acids with T3P® (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2,3-c]furan-1,3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue
Externí odkaz:
https://doaj.org/article/a77ff858a5594c65beef90ccce19fcab
Autor:
Ricarda Hannen, Lukas Biesen, Katrin Hoffmann, Ute Resch-Genger, Melanie Denißen, Guido J. Reiss, Thomas Müller, Nithiya Nirmalananthan-Budau, Dana Itskalov
Publikováno v:
Chemical Communications. 56:7407-7410
Merocyanine-triarylamine bichromophores are readily synthesized by sequentially Pd-catalyzed insertion-alkynylation-Michael-Suzuki four-component reactions. White-light emissive systems form upon aggregation in 1 : 99 and 0.1 : 99.9 vol% CH2Cl2-cyclo
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2340-2351 (2017)
In situ activation of 3-arylpropiolic acids with T3P® (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2,3-c]furan-1,3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue
Autor:
Melanie Denißen, Thomas Müller, Katrin Hoffmann, Ute Resch-Genger, Nithiya Nirmalananthan, Thomas Behnke
Publikováno v:
Materials Chemistry Frontiers. 1:2013-2026
A series of twelve 3-piperazinyl propenylidene indolone merocyanines was synthesized in a one-pot fashion using a consecutive three-component insertion-coupling-Michael addition sequence. Physical-organic treatment of the absorption data of a consang
Autor:
Aymelt Itzen, Norbert Schaschke, Uwe Beifuss, Matthias Lehmann, Anke Krueger, Florian Beuerle, Mathias O. Senge, Rolf Breinbauer, Christian Mück-Lichtenfeld, Thomas J. J. Müller, Melanie Denißen, Thomas Lindel, Jörg Pietruszka, Dennis Worgull, Tobias Gulder, Jan Paradies, Kilian Muñiz, Thorsten Bach, Klaus Ditrich, Christian Winter, Markus Kordes, Wolfgang von Deyn, Roland Pfau, Claudia Muhle-Goll, Burkhard Luy, Daniel B. Werz, Christoph Arenz, Wolfgang Hüttel, Jennifer N. Andexer, Bernd F. Straub
Publikováno v:
Nachrichten aus der Chemie. 64:255-294
Publikováno v:
European Journal of Organic Chemistry. 2015:5128-5142
(Pyrrol-3-yl)-1H-(aza)indazoles can be efficiently prepared by a two-step process that consists of a consecutive three-component coupling–cyclocondensation synthesis to give ortho-halo-3-acylpyrrol-3-yl-substituted (hetero)arenes followed by a cycl
Publikováno v:
RSC Advances. 5:33838-33854
1-, 3-, and 5-Biarylsubstituted pyrazoles can be efficiently prepared by a microwave-assisted consecutive four-component synthesis based upon a sequential Pd-catalyzed coupling–condensation–coupling (C3), a one-pot sequence which concatenates Son
Publikováno v:
ChemInform. 46
Autor:
Walter Frank, Jan Nordmann, Bernhard Mayer, Melanie Denissen, Thomas J. J. Mueller, Julian Dziambor
Publikováno v:
ChemInform. 46
1-, 3- and 5-biarylsubstituted pyrazoles are efficiently obtained by microwave-assisted consecutive four-component synthesis including a sequential Pd-catalyzed coupling-condensation-coupling, a one-pot sequence which combines Sonogashira alkynylatio
Publikováno v:
ChemInform. 46