104 research outputs found
Reduction of CO<sub>2</sub> into Methylene Coupled with the Formation of C–S Bonds under NaBH<sub>4</sub>/I<sub>2</sub> System
A selective four-electron
reduction of CO2 with thiophenol
using NaBH4 as a reductant is described to access dithioacetals.
This reaction provides a novel synthetic method for the highly selective
conversion of CO2 into methylene, and a new access to molecular
structures via formation of C–S bonds using CO2 as
the C1 source
N,N,O-Tridentate Mixed Lithium–Magnesium and Lithium–Aluminum Complexes: Synthesis, Characterization, and Catalytic Activities
The syntheses and crystal structures
of a series of heterobimetallic Li/Mg and Li/Al complexes prepared
from an N,N,O-tridentate ligand are described. The ligand HOC(CH2)5CH2N(Me)CH2CH2NMe2 (LH) and nBu2Mg
were used to synthesize the homometallic magnesium alkoxide [{LMgOC(CH2)5CH2N(Me)CH2CH2NMe2}2] (1), which
was reacted with nBuLi to afford the lithium alkylmagnesiate
[{Bu2Mg{LiOC(CH2)5CH2N(Me)CH2CH2NMe2}}2] (2). Complex 2 was then hydrolyzed to produce
[{BuMgOLi{LiOC(CH2)5CH2N(Me)CH2CH2NMe2}2}2] (3). The sequential reaction of LH in diethyl ether with RAlMe2 (R = Me, Cl) and nBuLi aforded two lithium aluminate complexes containing a
polymeric structure of one-dimensional chains [{−LiOC(CH2)5CH2N(Me)CH2CH2NMe2}Al(Me)(n-Bu)CH3−}n] (4) and [{−LiOC(CH2)5CH2N(Me)CH2CH2NMe2}Al(n-Bu)2CH2−}n] (5),
respectively. Each of the complexes 1–5 was structurally characterized and tested for its capability to
catalyze Meerwein–Ponndorf–Verley (MPV) reactions. Heterobimetallic
complexes 2 and 3 exhibited catalytic activities
better than those of homometallic magnesium complex 1 and heterobimetallic lithium aluminate complexes 4 and 5 for MPV reactions
Elimination of Chlorine (Radical) or Tosylate (Anion) from C2‘ of Nucleoside C3‘ Free Radicals as Model Reactions Postulated To Occur at the Active Site of Ribonucleotide Reductases<sup>1</sup>
Elimination of Chlorine (Radical) or Tosylate
(Anion) from C2‘ of Nucleoside C3‘ Free Radicals
as Model Reactions Postulated To Occur at the
Active Site of Ribonucleotide Reductases1</sup
Reduction of CO<sub>2</sub> with NaBH<sub>4</sub>/I<sub>2</sub> for the Conversion of Thiophenols to Aryl Methyl Sulfides
We report a tandem reaction to realize
reduction of carbon dioxide
with thiophenols to generate aryl methyl sulfides under the NaBH4/I2 system with 18-crown-6 as the solvent. Thiophenols
bearing electron-donating and electron-withdrawing groups are feasible
in this reaction. Controlled experiment results indicate that 18-crown-6
plays a critical role in six-electron reduction of carbon dioxide
Measure index on the set of Dow Jones index.
<p>Measure index on the set of Dow Jones index.</p
Diagram of (2D)<sup>2</sup>PCA+RBFNN forecasting model.
<p>The model is divided five modules, including the database of stock market, variables calculated module, sliding window, dimension reduction module and RBFNN predictor.</p
The input and output data of AICA-SVR model.
<p>The input and output data of AICA-SVR model.</p
The actual Dow Jones index and its predicted values from ICA-CCA-SVR, MICA-SVR, and AICA-SVR.
<p>The actual Dow Jones index and its predicted values from ICA-CCA-SVR, MICA-SVR, and AICA-SVR.</p
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