Umemoto Basic information
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Product Name:
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UmemotoII
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Synonyms:
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Umemoto;2,8-Difluoro-5-(trifluoromethyl)-5H-dibenzo[b,d]thiophen-5-ium Trifluoromethanesulfonate;Umemoto Reagent II;2,8-Difluoro-5-(trifluoromethyl)-5H-dibenzo[b,d]thiophen-5-ium Triflate;2,8-Difluoro-5-(trifluoromethyl)-1H-dibenzo[b,d]thiophen-5-ium Trifluoromethanesulfonate
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CAS:
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1961266-44-3
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MF:
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C14H6F8O3S2
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MW:
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0
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EINECS:
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Product Categories:
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Mol File:
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1961266-44-3.mol
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Umemoto Chemical Properties
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storage temp.
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Inert atmosphere,2-8°C
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Umemoto Usage And Synthesis
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Umemoto Preparation Products And Raw materials
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The once-elusive Ni(IV) species is now a potent candidate for challenging organic transformations
Sahni, Priya; Gupta, Rahat; Sharma, Simran; Pal, Amlan K. [Coordination Chemistry Reviews, 2023, vol. 474, art. no. 214849]
Abstract
The past few decades have witnessed a complete renaissance in the field of Ni(IV) catalysis. The properties of Ni(IV) complexes, such as, it undergoes rapid reductive elimination, slower β-hydride eliminations and its involvement in radical processes have permitted a broad range of innovative reaction development involving Ni(IV). The increasingly recognized unique properties of the Ni(IV) complexes have been leveraged to perform organic transformations which were long considered exceptionally complicated. The once elusive Ni(IV) species are now promoting a wide range of organic transformations in a complementary manner to the reactions involving Ni(0) and Ni(II) intermediates. The mechanistic description of a large number of Ni-catalyzed cross-coupling reactions has validated the involvement of high-valent Ni(IV) species in a large number of cross-coupling transformations, thus accessing new synthetic pathways with remarkable chemical activities. This comprehensive review spotlights the pivotal roles of isolated and/or spectroscopically identified Ni(IV) complexes. Amongst many applications, the Ni(IV) complexes have effectively been utilized in (i) C–heteroatom and C[sbnd]C bond formation, (ii) C[sbnd]H bond functionalization; and (iii) N[sbnd]N coupling reactions to forge heterocycles. Herein, we have demonstrated the accomplishments made in the field of organometallic Ni(IV) complexes in the last seven years, with a focus on the most recent and significant developments in the Ni(IV) catalysis emphasizing both synthetic outcomes and mechanisms.
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KCNT1 inhibitors and how to use them
Current Patent Assignee: PRAXIS PRECISION MEDICINES INC - KR2023/5168, 2023, A
Patent Family Members: AU2021241530 A1; BRPI2219041 A2; CA3176609 A1; CN115715189 A; EP4125831 A2; ...
Abstract
The present invention is directed to, in part, compounds and compositions useful for preventing and/or treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene (e.g., KCNT1). Methods of treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene such as KCNT1 are also provided herein.
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COMPOUND, COMPOSITION COMPRISING SAME, MOLDED PRODUCT, DYED PRODUCT, AND OPTICAL LAYER
Current Patent Assignee: SUMITOMO CHEMICAL COMPANY LIMITED; Dongwoo Fine-Chem (in: Sumitomo Chemical) - WO2023/287209, 2023, A1
Patent Family Members: WO2023/287209 A1; JP2023/13166 A; KR2023/131477 A; CN117177966 A
Abstract
The objective of the present invention is to provide a novel compound effectively absorbing light in a visible light range and, simultaneously, having excellent weather resistance. The present invention provides: a compound, which has cations comprising a partial structure represented by formula (I); a composition comprising same; a molded product; a dyed product; and an optical layer.
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