Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Long-Tao Huang"'
Autor:
Long-Tao Huang, Yuta Kitakawa, Kodai Yamada, Futa Kamiyama, Masahiro Kojima, Tatsuhiko Yoshino, Shigeki Matsunaga
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb53487ae6d53da9418bed3e432e6f6c
https://doi.org/10.1002/ange.202305480
https://doi.org/10.1002/ange.202305480
Autor:
Yuki Hirata, Masahiro Kojima, Yoshimi Kato, Long-Tao Huang, Shigeki Matsunaga, Tatsuhiko Yoshino, Luqing Lin
Publikováno v:
Synthesis. 54:4703-4710
Ruthenium(II)-catalyzed enantioselective C–H functionalization reactions of sulfoximines with sulfoxonium ylides are described. The combination of [RuCl2(p-cymene)]2 and a pseudo-C 2-symmetric binaphthyl monocarboxylic acid furnished the S-chiral p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c903e4dca0f3778629b0c3af92d6a7b
https://doi.org/10.1055/a-1588-0072
https://doi.org/10.1055/a-1588-0072
Publikováno v:
Organic Letters. 22:8256-8260
The enantioselective C-H alkylation of 8-ethylquinolines with enones or acrolein using a RhIII catalyst and a chiral carboxylic acid is described. Under mild reaction conditions, a binaphthyl-based chiral carboxylic acid enables the enantioselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75e892b9d4554265acbece8b60f94210
https://doi.org/10.1021/acs.orglett.0c02872
https://doi.org/10.1021/acs.orglett.0c02872
Publikováno v:
Organic letters. 22(21)
The enantioselective C-H alkylation of 8-ethylquinolines with enones or acrolein using a Rh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::588a59ccdcd457fa31a4d0346eaea819
https://pubmed.ncbi.nlm.nih.gov/33064493
https://pubmed.ncbi.nlm.nih.gov/33064493
Autor:
Longqing Zhu, Long-Tao Huang, Jinhong Chen, Jiao-Xia Zou, Yuhang Yang, Yi Jiang, Xue Peng, Yongqiang Wang, Yiyue Feng, Zhen Wang
Publikováno v:
Organic Chemistry Frontiers. 5:2317-2321
A new and practical approach to α-dithioacetal/α-diselenoacetal amides has been developed, combining sequential functionalization of amides and a C–C bond cleavage strategy. In this reaction, various α-dithioacetal/α-diselenoacetal amides from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c49ac5af848efa7e23658b9030cf9712
https://doi.org/10.1039/c8qo00435h
https://doi.org/10.1039/c8qo00435h
Autor:
Xue-Qiang Wang, Longqing Zhu, Long-Tao Huang, Honghua Zhang, Yingmei Lu, Yongqiang Wang, Quanyi Zhao, Yiyue Feng, Zhen Wang
Publikováno v:
Chemical Communications. 54:8265-8268
A new approach for the synthesis of isatins and isoindigoes by an inexpensive and environmentally friendly NaI-mediated transformation is disclosed. The selectivity could be switched by simply varying the solvent, and isatins (using THF) and isoindig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e732b9ff4d01beb37147bbb2289a702
https://doi.org/10.1039/c8cc04471f
https://doi.org/10.1039/c8cc04471f
Autor:
Yuhang Yang, Xue Peng, Longqing Zhu, Yiyue Feng, Yi Jiang, Long-Tao Huang, Xiao-Yun Zhang, Zhen Wang, Jiedan Deng, Jiao-Xia Zou
Publikováno v:
Organicbiomolecular chemistry. 16(10)
An efficient and practical methodology to obtain α-thio-β-dicarbonyl compounds was presented under alkaline conditions via potassium iodide (KI) catalysis; various symmetrical/unsymmetrical 1,3-dicarbonyl compounds were obtained under an aerobic at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d344d5c8b2abbd546987173fb2aeb060
https://pubmed.ncbi.nlm.nih.gov/29461552
https://pubmed.ncbi.nlm.nih.gov/29461552
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundTranscription factors (TFs) play a crucial role in tumorigenesis and anti-tumor immunity. However, the potential role of large-scale transcription factor regulation patterns in the progression in gastric cancer (GC) is unknown.MethodsWe com
Externí odkaz:
https://doaj.org/article/5f0a65af0f49442ebd889b0d6dd0f8ee