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961.
Dr. Tobias Michael Milzarek Prof. Dr. Jerome Waser 《Angewandte Chemie (International ed. in English)》2023,62(33):e202306128
The first trifluoromethylation of vinylbenziodoxolones (VBX) is reported herein. The synthetic method is based on the use of bench-stable, high-valent copper(III) species, and the reaction can be initiated under thermal conditions and/or irradiation (365 nm) giving access to trifluoromethylated alkenes in a stereoselective fashion. Various VBX reagents derived from tyrosine, cysteine, small peptides, thiols and amides can be used as precursors. The obtained alkenes could be further functionalized by reduction or epoxidation of the trifluoromethylated double bond. Furthermore, the method could be applied in a large-scale batch/flow synthesis and could be conducted under visible light irradiation. 相似文献
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Lijuan J. Wang Margaret L. Grapperhaus Barnett S. Pitzele Timothy J. Hagen Kam F. Fok Jeffrey A. Scholten Dale P. Spangler Mihaly V. Toth Gina M. Jerome William M. Moore Pamela T. Manning James A. Sikorski 《Heteroatom Chemistry》2002,13(1):77-83
The efficient syntheses of two new types of conformationally constrained S‐[2‐[(1‐iminoethyl)amino]ethyl]homocysteine derivatives, 1‐amino‐3‐[2[(1‐iminoethyl)amino]ethylthio]cyclobutane carboxylic Acid ( 5 ) and (4S)‐4‐[[2‐[(1‐Iminoethyl)amino]ethyl]thio]‐L‐proline ( 6 ), are reported. These molecules represent the first attempts to probe conformational constraint near the α‐amino acid moiety of known homocysteine‐based inhibitors of nitric oxide synthase. Targets 5 and 6 were evaluated as potential inhibitors of the three human isoforms of nitric oxide synthase. © 2002 John Wiley & Sons, Inc. Heteroatom Chem 13:77–83, 2002; DOI 10.1002/hc.1109 相似文献
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Dr. Nieves P. Ramirez Prof. Dr. Jerome Waser 《Angewandte Chemie (International ed. in English)》2023,62(32):e202305776
An asymmetric 3-component reaction between EthynylBenziodoXoles (EBXs), 2,2,2-trifluorodiazoethane and nucleophiles catalyzed by a CuI-BOX (Bisoxazoline) catalyst is described. This protocol gives access to chiral trifluoromethylated propargyl ethers and anilines, which are valuable building blocks in synthetic and medicinal chemistry. The reaction proceeds with high enantioselectivity and yield with different nucleophiles such as primary, secondary and tertiary alcohols, as well as both electron-rich and electron-poor anilines. Aryl-, alkyl- and silyl-substituted alkynes can be successfully introduced as electrophiles. In case of chiral substrates, high catalyst control was observed, leading to good diastereoselectivity. 相似文献
967.
J. Mary Linet S. Dinakaran S. Mary Navis Priya S. Jerome Das 《Crystal Research and Technology》2009,44(2):173-176
Semiorganic single crystals of thiosemicarbazide cadmium chloride (TSCCC) and mercury ions doped thiosemicarbazide cadmium chloride were synthesized by slow solvent evaporation technique. The grown crystals were subjected to powder X‐ray analysis and both the crystals were found to crystallize in the monoclinic system. EDAX analysis was carried out for chemical analysis of the grown crystals. The UV‐Vis‐NIR spectrum shows that both the materials have wide transparency window in the visible and near IR region. The dielectric studies were carried out to estimate the dielectric constant and dielectric loss with respect to frequency for both the crystals. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
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