Access to novel imidazo[1,5-a]pyrazine scaffolds by the combined use of a three-component reaction and a base-assisted intramolecular cyclization-Reference-Cited by-同舟云学术

Access to novel imidazo[1,5-a]pyrazine scaffolds by the combined use of a three-component reaction and a base-assisted intramolecular cyclization

Author:

Attanasi Orazio A.¹²³⁴,Favi Gianfranco¹²³⁴,Giorgi Gianluca⁵⁶⁷,Majer Roberta¹²³⁴,Perrulli Francesca Romana¹²³⁴,Santeusanio Stefania¹²³⁴

Affiliation:

1. Department of Biomolecular Sciences

2. Section of Organic Chemistry and Organic Natural Compounds

3. University of Urbino “Carlo Bo”

4. 61029 Urbino, Italy

5. Department of Chemistry

6. University of Siena

7. 53100 Siena, Italy

Abstract

A novel and practical two-step approach to an intriguing class of imidazo[1,5-a]pyrazines with exocyclic CX (X = CH₂, O) bonds is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

Reference62 articles.

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