Literature DB >> 21589958

Imides: forgotten players in the Ugi reaction. One-pot multicomponent synthesis of quinazolinones.

Riccardo Mossetti1, Tracey Pirali, Dèsirèe Saggiorato, Gian Cesare Tron.   

Abstract

Up to now, the synthesis of quinazolinones has required lengthy synthetic procedures. Here, we describe an innovative one-pot multicomponent reaction leading to highly substituted quinazolinones. We believe that this novel transformation may open the door for the generation of new and pharmacologically active quinazolinones, but, most important of all, the resurrection of the imide-Ugi scaffold paves the way for the synthesis of novel molecular architectures. This journal is © The Royal Society of Chemistry 2011

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21589958     DOI: 10.1039/c1cc12067k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  General one-pot, two-step protocol accessing a range of novel polycyclic heterocycles with high skeletal diversity.

Authors:  Zhigang Xu; Muhammad Ayaz; Alexandra A Cappelli; Christopher Hulme
Journal:  ACS Comb Sci       Date:  2012-07-12       Impact factor: 3.784

2.  Telescoped synthesis of C3-functionalized (E)-arylamidines using Ugi-Mumm and regiospecific quinazolinone rearrangements.

Authors:  Victor A Jaffett; Alok Nerurkar; Xufeng Cao; Ilia A Guzei; Jennifer E Golden
Journal:  Org Biomol Chem       Date:  2019-03-20       Impact factor: 3.876

3.  Diastereoselective, Multicomponent Synthesis of Pyrrolopyrazinoquinazolinones via a Tandem Quinazolinone Rearrangement/Intramolecular Ring Closure of Tautomeric (Z)-Benzamidines.

Authors:  Victor A Jaffett; Jhewelle N Fitz-Henley; Muhammad M Khalifa; Ilia A Guzei; Jennifer E Golden
Journal:  Org Lett       Date:  2021-07-12       Impact factor: 6.072

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.