Zobrazeno 1 - 10
of 583
pro vyhledávání: '"Lars May"'
Autor:
Tan, Yuting1,2,3, Deng, Wenhui1,2,3, Liu, Tianshu1,2,3, Huang, Lei1,2,3, Zhang, Ruize1,2,3, Zhang, Yichan1,2,3, Fu, Yanan1,2,3, Fang, Lingyun1,2,3, Li, Yuman1,2,3, Zhang, Li1,2,3, Xie, Mingxing1,2,3 xiemx@hust.edu.cn, Wang, Jing1,2,3 jingwang2004@hust.edu.cn
Publikováno v:
Echocardiography. Nov2023, Vol. 40 Issue 11, p1243-1250. 8p.
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8031d96c3a8f7dab10e479c623f503b
http://europepmc.org/articles/PMC8518837
http://europepmc.org/articles/PMC8518837
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,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457fcce5c51dc2ba6e4b4e3d4508282e
https://doi.org/10.1002/chem.202000859
https://doi.org/10.1002/chem.202000859
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c604c3d29b509fcd1d73fa00aa15328
http://europepmc.org/articles/PMC7540341
http://europepmc.org/articles/PMC7540341
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f01d23af1421f94aa04235f8ecb06f
https://doi.org/10.1039/c9qo01318k
https://doi.org/10.1039/c9qo01318k
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::105f97594f6a3f2f9b4992acc949e53c
https://doi.org/10.1039/d0qo00182a
https://doi.org/10.1039/d0qo00182a
Publikováno v:
Dyes and Pigments. 206:110564
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ee0d8ded56697033bd64e93a4fa546e
https://doi.org/10.1016/j.dyepig.2022.110564
https://doi.org/10.1016/j.dyepig.2022.110564
Autor:
Chen, Buxin1 (AUTHOR), Zhang, Zheng1 (AUTHOR), Xia, Dan1 (AUTHOR), Sidky, Emil Y.1 (AUTHOR), Gilat-Schmidt, Taly2 (AUTHOR), Pan, Xiaochuan1,3 (AUTHOR) xpan@uchicago.edu
Publikováno v:
Bioengineering (Basel). Dec2022, Vol. 9 Issue 12, p775. 18p.