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This work is supported by the National Natural Science Foundation of China(No.21902083);the Natural Science Foundation of Shandong Province(No.ZR2020QB130);This work is also supported by the Talent Program Foundation of Qufu Normal University(Nos.6132 and 6125).
Chloroalkanes are important building blocks in the synthesis,but their use in redox chemistry is limited by their negative reduction potentials.Electrosynthesis can precisely control the reaction energy just by adjust...
The reaction of imidazole-2-thione derivative 1 with 2-chloro-N-p-tolylacetamide afforded the corresponding 2-(1HI-imidazol-2-ylthio)-N-p-tolylacetamide 2. Reaction compound 2 with different reagents such as p-chlorob...
the Razi University Research Council for partial support of this work
A simple and efficient protocol for the deprotection of dithioacetal,1,3-dithianes and 1,3-dithiolanes has been developed using H_2O_2-SOC1_2 reagent system.In addition to the absence of overoxidation products for oxi...
Project supported by the National Natural Science Foundation of China (No. 20272008) and the Key Grant Project of Chinese Mimstry of Eucation (No. 10412).
Under basic conditions, a series of 4,4-dialkylthio-l,2-diaza-l,3-butadienes were synthesized in good to excellent yields via a novel azo-coupling decarboxylation reaction by reacting a-carboxyl ketene dithioacetals w...
Supported by the National Natural Science Foundation of China(No. 29862004) ;Scientific and Technological DevelopmentProgram Foundation of Jilin Province(No. 20040565).
α-Oxoketene dithioacetals( compound 1 ) are versatile synthons for organic synthesis due to their specially structural characteristic, that is, the masked ketene is conjugated with the convertible carbonyl in their...
The title compounds 3 and 4 condensed with aromatic aldehydes to give a--aroylsicinnamoyl ketene cyclic dithioacetals 5 and 6 with sodium ethoxide as the base. The stereochemistryofs and 6 was assigned as E-configurat...
Cyclic dithioacetals of α,α-dioxo (estcr) ketene 3 were reacted with butanone to afford the Michael adducts 4, catalyZed by metal Na. This process provides a new method for the Synthesis of ring-compouds in goob yie...
The addition reaction of Grignard reagents to a-cinnamoyl ketene(l,3propylene) dithoacetals was performed . The experiments show that the addition proceeds completely in a conjugated l,4-manner. Possible mechanism fo...
The addition teaction of Grignard reagents to a-cinnamoyl ketene (1, 2-ethylene) dithioncetals 4 was examined.The results showed that the 1, 4-manner nucleoohilie attack at the cinnamoyl carbon double bond occurred. P...
The dihydric dithioketenes 3a-c obtained by 1,2-addition of methallyl Grignard reagent to bis(alkylthio)methylidene derivative ofdimedone 2a-c wewr converted to the cycloaromatization product 4 assisted by boron trifl...