2015
DOI: 10.1055/s-0034-1380231
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Trimethylsilyl Cyanide (TMSCN)

Abstract: was born in 1988 in Puebla, Mexico. She obtained her B.Sc. degree in Chemistry (2011) and her M.Sc. degree in organic chemistry (2014) from Benemérita Universidad Autónoma de Puebla. Currently she works towards her Ph.D. under the guidance of Professor Sara Montiel Smith and Professor Penélope Merino Montiel. Her research focuses on the synthesis of steroidal spiro heterocycles.

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Cited by 3 publications
(5 citation statements)
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“…The anticancer activity of compounds 3 . It should be noted that only white deposition was obtained without the presence of HNO 3 , indicating the HNO 3 might act as a pH regulator which is very important for the formation of the water soluble Gd 3+ ions in the reaction process.…”
Section: Mtt Assaymentioning
confidence: 99%
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“…The anticancer activity of compounds 3 . It should be noted that only white deposition was obtained without the presence of HNO 3 , indicating the HNO 3 might act as a pH regulator which is very important for the formation of the water soluble Gd 3+ ions in the reaction process.…”
Section: Mtt Assaymentioning
confidence: 99%
“…[2] Trimethylsilyl cyanide (TMSCN) is one of the most useful and safe cyanating reagents for nucleophilic addition to carbonyl compounds to give cyanohydrin trimethylsilyl ethers. [3] Hence, the development of efficient catalysts for cyanosilylation of carbonyl compounds with TMSCN is a very important subject in current research, and several efficient catalysts have been developed so far. During the past few decades, a lot of organic catalysts have been developed for the cyanosilylation of carbonyl compounds with TMSCN, but these catalysts suffer from some drawbacks such as tedious separation and recycle problems, which restrict their practical applications.…”
Section: Introductionmentioning
confidence: 99%
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“…According to the traditional Kornblum’s rule, which is applied for prediction of the regioselectivity of ambident nucleophiles, the N -terminus of cyanide preferentially reacts in the S N 1-type substitution. However, even in those reactions, the C -terminus of the cyanide reacts prior to the N -terminus, because the formation of the nitrile is both kinetically and thermodynamically more favorable in most cases. , Therefore, development of a selective synthetic method of isonitrile by the nucleophilic substitution is highly desirable . Realizing such a method by the catalytic procedure is more challenging.…”
mentioning
confidence: 99%