Organic Chemistry of Sulfur 1977
DOI: 10.1007/978-1-4684-2049-4_11
|View full text |Cite
|
Sign up to set email alerts
|

Sulfinic Acids and Sulfinic Esters

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
9
0

Year Published

1980
1980
2021
2021

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 18 publications
(9 citation statements)
references
References 100 publications
0
9
0
Order By: Relevance
“…This procedure made use of a mobile phase of 7:3 95% ethanohwater (saturated atmosphere) and a stationary phase of Silica Gel-G. Elution times were 35-45 min. Low molecular weight sulfinic acids are air-oxidized (20). This reaction occurs during the development of the chromatogram and complicates the results.…”
Section: Methodsmentioning
confidence: 99%
“…This procedure made use of a mobile phase of 7:3 95% ethanohwater (saturated atmosphere) and a stationary phase of Silica Gel-G. Elution times were 35-45 min. Low molecular weight sulfinic acids are air-oxidized (20). This reaction occurs during the development of the chromatogram and complicates the results.…”
Section: Methodsmentioning
confidence: 99%
“…However, less review was reported. In 1977, Oae and Kunieda [1a] provided an overview of sulfinic acids and sulfinic esters. A lot of methodologies about sulfinic acids have emerged in recent years.…”
Section: Introductionmentioning
confidence: 99%
“…which the positive charge delocalized on the aromatic ring could explain the MeSO, -anion nuclear attack. Although this would fit the formation of (k), (&), (Sc), or (12), the recovery of (7) (sulphonylation at a non-conjugated position) and the methyl substitution in (&) seem harder to explain.…”
mentioning
confidence: 94%