2015
DOI: 10.3987/com-14-13154
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of N-Substituted (Z)-3-Arylbenzo[c]thiophen-1(3H)-imines by the Reaction of 1-[Aryl(methoxy)methyl]-2-lithiobenzenes with Isothiocyanates Followed by Acid-Mediated Cyclization

Abstract: The title transformation provides benzothiophenimines some of which are further hydrolized to the corresponding benzothiophenones.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2015
2015
2017
2017

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(1 citation statement)
references
References 12 publications
0
1
0
Order By: Relevance
“…Whereas these compounds are typically synthesized through multistep processes or by nucleophilic additions onto thiophthalic anhydride, ,,, the restricted available methods for their preparation have most likely hampered their use in medicinal chemistry. Accordingly, in order to allow a more thorough evaluation of the pharmacological potential of this so far overlooked chemical space, the development of new synthetic methods is highly desirable.…”
mentioning
confidence: 94%
“…Whereas these compounds are typically synthesized through multistep processes or by nucleophilic additions onto thiophthalic anhydride, ,,, the restricted available methods for their preparation have most likely hampered their use in medicinal chemistry. Accordingly, in order to allow a more thorough evaluation of the pharmacological potential of this so far overlooked chemical space, the development of new synthetic methods is highly desirable.…”
mentioning
confidence: 94%