Synthesis of new substituted thieno[2,3-d]imidazolone from hydantoin

Ba, Lalla A.; Kirsch, Gilbert; Castello, Jérémie

doi:10.3998/ark.5550190.0008.a25

Search citation statements

Order By: Relevance

Paper Sections

Select...

Formylation and Chlorination1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2023

Publication Types

Select...

Article1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 1 publication

(1 citation statement)

References 5 publications

(6 reference statements)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The preparation of the key intermediate 108 in this reaction was accomplished via the Vilsmeier–Haack reaction of 1,3-dibenzyl-2,4-imidazolidinedione 107 (Scheme 34 ). 66 The 1,3-dibenzyl-2,4-imidazolidinedione 108 can then be transformed into thieno[2,3- d ]imidazolones 109 .…”

Section: Formylation and Chlorinationmentioning

confidence: 99%

Synthetic Utility of the Vilsmeier–Haack Reagent in Organic Synthesis

Singh

Dohi

Kumar

et al. 2023

Synlett

View full text Add to dashboard Cite

The Vilsmeier–Haack reaction has historically been a topic of significant interest to organic chemists, and it continues to attract considerable attention. The reaction itself provides a facile route towards a large number of aromatic and heteroaromatic systems. The Vilsmeier–Haack reagent, generated from amides and halides, is found to be very important in organic synthesis. This account highlights recent developments in the synthetic utility of the Vilsmeier–Haack reagent.1 Introduction2 Formylation3 Formylation and Chlorination4 Formylation and Acetylation5 Chlorination6 ortho-Formylation7 Miscellaneous8 Conclusions

show abstract

Section: Formylation and Chlorinationmentioning

confidence: 99%