Questions tagged [organocatalysis]
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What is the inherent mechanism in carbocatalysis?
When checking non-metallic catalysis materials, one mentioned example is that of carbocatalysis; using heterogeneous carbon structure to catalyze a reaction (Not to be confused as a support surface ...
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When does the Mukaiyama-Addition follow which transition state and how does it affect the stereochemistry?
in the course on enantioselective organocatalysis, we discussed the route to hexoses via organocatalytic aldol addition and subsequent Mukaiyama addition. The use of either TiCl4 or MgBr2 leads to ...
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Advantages of p-toluenesulfonic acid over sulfuric acid in the formation of acetals
I am currently working on an undergraduate experiment to form a cyclic acetal.
We were asked to use p-toluenesulfonic acid as a catalyst rather than sulfuric acid.
This seems to be common practice ...
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What is the product when cyclohexanone reacts with morpholine?
The question asked to find the final product of the reaction between cylohexanone and morpholine. I attempted the reaction which is shown below:
I have understood the heat symbol. It simply ...
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Organic-catalysis microwaves [closed]
When we perform a organic reaction without any addtional catalyst except that the reaction is carried out under microwave condition we can accelerate this reaction in comparison with one under heating ...
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Does Raney nickel deprotect acetals?
I know that Raney nickel can deprotect thioacetals. Can it deprotect acetals as well?
I found this image which shows that it deprotects and removes many protecting groups. But there was no reference ...
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Constraints on rate coefficients in chiral catalytic system
Consider some reversible chemical reaction in a closed system:
$$\ce{A <=> B + D} \tag{1}$$
where $\ce{A}$ is some input reagent and $\ce{B}$, $\ce{D}$ are some output reagents. Let's denote ...
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Why is nitrosobenzene electrophilic on O in organocatalytic oxygenations?
In 2003 Zhong1 and MacMillan2 reported the use of nitrosobenzene, PhNO, in the organocatalytic asymmetric α-oxygenation of carbonyl compounds:
which is all nice, except for the slightly ...
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