Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR process

Fabio De Moliner; Christopher Hulme

doi:10.1021/ol3003282

Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR process

Fabio De Moliner, Christopher Hulme

Research output: Contribution to journal › Article › peer-review

59 Scopus citations

Abstract

An efficient multicomponent-based methodology providing a new entry into a medicinally important complex heterocyclic core is presented. The strategy is very general and able to endow target compounds with the highest possible number of diversity points. Notably, four new chemical bonds and two aromatic rings are formed in a one-pot fashion.

Original language	English (US)
Pages (from-to)	1354-1357
Number of pages	4
Journal	Organic Letters
Volume	14
Issue number	5
DOIs	https://doi.org/10.1021/ol3003282
State	Published - Mar 2 2012

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol3003282

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title = "Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR process",

abstract = "An efficient multicomponent-based methodology providing a new entry into a medicinally important complex heterocyclic core is presented. The strategy is very general and able to endow target compounds with the highest possible number of diversity points. Notably, four new chemical bonds and two aromatic rings are formed in a one-pot fashion.",

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AB - An efficient multicomponent-based methodology providing a new entry into a medicinally important complex heterocyclic core is presented. The strategy is very general and able to endow target compounds with the highest possible number of diversity points. Notably, four new chemical bonds and two aromatic rings are formed in a one-pot fashion.

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Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR process

Abstract

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