2022
DOI: 10.1039/d2ob01069k
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of functionalized S-benzyl dithiocarbamates from diazo-compounds via multi-component reactions with carbon disulfide and secondary amines

Abstract: Triflic acid promoted multi-component synthesis of functionalized S-benzyl dithiocarbamates from diazo compounds, carbon disulfide and secondary amines is reported. The reactions proceeded at room temperature and gave the desired dithiocarbamates...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
2
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 11 publications
(2 citation statements)
references
References 52 publications
0
2
0
Order By: Relevance
“…activities. 31,32 Prominent among these are S-benzyl esters 33 as are pyrrolidine dithiocarbamates. [34][35][36] As an extension of work exploring the potential biological activity of metal dithiocarbamates, including pyrrolidine derivatives, [37][38][39] and systematic studies of molecules that differ only in the nature of a small substituent, [40][41][42][43] a series of five S-benzyl esters of pyrrolidine dithiocarbamate were investigated which differ in the nature of the substituent in the 4-position of the terminal phenyl group.…”
Section: Introductionmentioning
confidence: 99%
“…activities. 31,32 Prominent among these are S-benzyl esters 33 as are pyrrolidine dithiocarbamates. [34][35][36] As an extension of work exploring the potential biological activity of metal dithiocarbamates, including pyrrolidine derivatives, [37][38][39] and systematic studies of molecules that differ only in the nature of a small substituent, [40][41][42][43] a series of five S-benzyl esters of pyrrolidine dithiocarbamate were investigated which differ in the nature of the substituent in the 4-position of the terminal phenyl group.…”
Section: Introductionmentioning
confidence: 99%
“…It is well-known that the reaction of primary amine with CS 2 affords corresponding dithiocarbamic acid. 12 In our reaction system, however, the addition of the dithiocarbamic acid to 2 unlikely occurs since it requires a Cu( ii )/O 2 catalyst for the more simple case of pristine [60]fullerene. 12 a Therefore, 3 is considered to be formed via an alternative scheme (Fig.…”
mentioning
confidence: 99%