2014
DOI: 10.6023/cjoc201312020
|View full text |Cite
|
Sign up to set email alerts
|

Acidity-Controlled Indolylation of 3, 3-Bis(ethylthio)acrylate

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2015
2015
2021
2021

Publication Types

Select...
5

Relationship

2
3

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 14 publications
(14 reference statements)
0
3
0
Order By: Relevance
“…The specific surface area of the catalysts exhibited a unique trend with the increase of K content, which first increased to 177.1 m 2 /g due to the improved dispersion of microcrystalline particles and the reduced particle size, following decrease to 156.2 m 2 /g owing to the K monomer layer generated on the iron surface. This phenomenon has been certified by You et al [ 38 ]…”
Section: Resultsmentioning
confidence: 54%
See 1 more Smart Citation
“…The specific surface area of the catalysts exhibited a unique trend with the increase of K content, which first increased to 177.1 m 2 /g due to the improved dispersion of microcrystalline particles and the reduced particle size, following decrease to 156.2 m 2 /g owing to the K monomer layer generated on the iron surface. This phenomenon has been certified by You et al [ 38 ]…”
Section: Resultsmentioning
confidence: 54%
“…[ 35,36 ] Xiong et al [ 37 ] proved that the Fe/CNT catalysts promoted by potassium and sodium not only suppressed the production of methane but also increased the distribution of olefins and selectivity of C 5+ in FTS reaction. You et al [ 38 ] found that adding alkali metals to non‐supported Fe‐based catalysts could significantly improve the CO 2 conversion and C 5+ selectivity. Specifically, the catalysts modified by K and Rb achieved better performance.…”
Section: Introductionmentioning
confidence: 99%
“…-Ethylthio--indolyl-,-unsaturated ketones 1 are readily prepared by trifluoroacetic acid or iron(III) chloride mediated selective desulfitative carbon-carbon cross-coupling reaction of indoles and -oxoketene dithioacetals. 17,[23][24][25] In order to obtain optimal reaction conditions for complementary and regioselective synthesis of both 3 and 4, we commenced our investigation on the cyclocondensation of 1a (0.25 mmol) and hydroxylamine hydrochloride (2; 0.5 mmol) as model substrates (Table 1). Initially, the cyclocondensation reaction was performed in the presence of NaOEt (0.75 mmol, 3 equiv) in refluxing EtOH for 8 h, affording the desired product 3a in 88% yield (Table 1, entry 1), which was confirmed by spectral and analytical data as well as comparison with the authentic sample.…”
Section: Paper Synthesismentioning
confidence: 99%