Solvent-Free Oxidation of Secondary Alcohols to Carbonyl Compounds by 1, 3-Dibromo-5, 5-Dimethylhydantoin (DBDMH) and 1, 3-Dichloro-5, 5-Dimethylhydantoin (DCDMH)
نویسندگان
چکیده
منابع مشابه
Number 2 - 1 3 - 1 4 - 1 5 - 1 5 - 2 5 - 3 5 - 4 5 - 5 5 - 6 5 - 7 5 - 8 6 - 1 •
A decentralized failure detection and isolation (FDI) methodology, which is robust with respect to model uncertainties and noise, is presented. Redundancy metrics are developed, and optimization problems are posed for the choices of robust parity relations. Closed-form solutions for some special failure cases are given. Connections are drawn with other disciplines, and the use of the metrics to...
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In the title compound, C(15)H(9)Br(2)Cl(2)FO, the dihedral angle between the two aromatic rings is 6.0 (1)°. The dibromo-ethane fragment of the propan-1-one unit is disordered over two positions, with occupancies of ca 0.83 and 0.17. The crystal structure is stabilized by inter-molecular C-H⋯O hydrogen bonds, C-H⋯π inter-actions, and Br⋯Cl [3.505 (2) and 3.576 (6) Å] and Cl⋯F [3.176 (2) Å] shor...
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A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
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A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
متن کاملسنتز 1، 3، 5، 7-تترا استیل-1، 3، 5، 7-تترا آزاسیکلواکتان (TAT) از طریق استیل‌دار کردن 3، 7-دی‌استیل-1، 3، 5، 7-تترا آزا بی‌سیکلو-[3.3.1]-نونان (DAPT)
In this study, a novel method to synthesis of 1,3,5,7-tetraacetyl octahydro-1,3,5,7-tetraazocine or 1,3,5,7-tetraacetyl-1,3,5,7-tetraazacyclooctane (TAT) was used through acetolysis of 3,7-diacetyl-1,3,5,7-tetraazabicyclo-[3.3.1]nonane (DAPT) with acetic anhydride in the presence of sodium acetate as catalyst. Optimized reaction conditions were obtained by changing temperature, time and startin...
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ژورنال
عنوان ژورنال: Journal of the Brazilian Chemical Society
سال: 2013
ISSN: 0103-5053
DOI: 10.5935/0103-5053.20130304