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pro vyhledávání: '"Lars May"'
Publikováno v:
Catalysts, Vol 10, Iss 12, p 1412 (2020)
A series of novel 3- and 5-biaryl-substituted isoxazoles was prepared by a rapid microwave-assisted four-component three-step synthesis: concatenating Sonogashira coupling, cyclocondensation, and Suzuki coupling in a one-pot fashion. The Pd-catalyst
Externí odkaz:
https://doaj.org/article/521e3f8628484d9f94be166131c50380
Autor:
Lars May, Thomas J. J. Müller
Publikováno v:
Molecules, Vol 25, Iss 9, p 2180 (2020)
This mini-review summarizes the syntheses and functionalizations of dithieno[1,4]thiazines and bis[1]benzothieno[1,4]thiazines, both electron density-enriched congeners of phenothiazines with remarkable electronic properties. Diversity-oriented, stra
Externí odkaz:
https://doaj.org/article/bf8601d6f3c84f23baa5d5d0417f4bd1
Autor:
Thomas Müller, Lars May, Ute Resch-Genger, Katrin Hoffmann, Nithiya Nirmalananthan-Budau, Lukas Biesen
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Aroyl‐S,N‐ketene acetal‐based bichromophores can be readily synthesized in a consecutive three‐component synthesis in good to excellent yields by condensation of aroyl chlorides and an N‐(p‐bromobenzyl) 2‐methyl benzothiazolium salt fol
Autor:
Lars May, Thomas Müller
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
2,6‐Difunctionalized dithieno[1,4]thiazines were efficiently synthesized by (pseudo)five‐ or (pseudo)three‐component one‐pot processes based on lithiation‐electrophilic trapping sequences. As supported by structure–property relationships,
Autor:
Lars May, Thomas Müller
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A series of isomeric dithieno[1,4]thiazines is accessible through an intermolecular–intramolecular Buchwald–Hartwig amination starting from dihalodithienyl sulfides. The electronic properties of dithieno[1,4]thiazine isomers differ conspicuously
Publikováno v:
Organic Chemistry Frontiers. 7:329-339
Functional thiophenes, e.g. for organic metal-free dye sensitized solar cells (DSSC), are accessible efficiently via a divergent and diversity-oriented synthetic strategy. Here, we present two straightforward, modular and comparative one-pot synthese
Publikováno v:
Organic Chemistry Frontiers. 7:1206-1217
A broad series of electronically diverse N-aryl substituted phenothiazines was readily synthesized by Buchwald–Hartwig amination of 10H-phenothiazine and aryl bromides with variable electronic nature in moderate to excellent yields (61–97%). This
Publikováno v:
Dyes and Pigments. 206:110564
Publikováno v:
Catalysts
Volume 10
Issue 12
Catalysts, Vol 10, Iss 1412, p 1412 (2020)
Volume 10
Issue 12
Catalysts, Vol 10, Iss 1412, p 1412 (2020)
A series of novel 3- and 5-biaryl-substituted isoxazoles was prepared by a rapid microwave-assisted four-component three-step synthesis: concatenating Sonogashira coupling, cyclocondensation, and Suzuki coupling in a one-pot fashion. The Pd-catalyst
Autor:
Lars May, Thomas J. J. Müller
Publikováno v:
Chemistry – A European Journal. 26