Literature DB >> 11281825

The multicomponent reactions and their libraries for natural and preparative chemistry.

I Ugi1, S Heck.   

Abstract

It was recently recognized that three different types of multi-component reactions (MCRs) exist. In preparative chemistry, the MCRs of type II form their products particularly efficiently. These reactions correspond to equilibria of educts and intermediate products, whose final products are formed practically irreversibly. In recent years, the four component reaction of the isocyanides (U-4CR) of type II and their unions with various reactions and MCRs have become an important industrial process for preparing products and their libraries. It has been demonstrated that all conceivable collections of U-4CR educts can be converted into the corresponding products. In the usual chemical reactions, only the substituents of the products can be varied, whereas the U-4CR and related reactions can also produce skeletally different types of products with diverse substituents. The preparative advantages of forming products by the one-pot MCRs and the great variety of the possible products are illustrated in this review.

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Year:  2001        PMID: 11281825     DOI: 10.2174/1386207013331291

Source DB:  PubMed          Journal:  Comb Chem High Throughput Screen        ISSN: 1386-2073            Impact factor:   1.339


  14 in total

1.  A multi-component reaction (MCR) approach to the synthesis of highly diverse polymers with polypeptide-like features.

Authors:  Claude V Robotham; Christopher Baker; Brian Cuevas; Khalil Abboud; Dennis L Wright
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

2.  High pressure: a promising tool for multicomponent reactions.

Authors:  Leon W A van Berkom; George J T Kuster; Hans W Scheeren
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

3.  Improved synthesis of 15-deoxyspergualin analogs using the Ugi multi-component reaction.

Authors:  Christopher G Evans; Matthew C Smith; James P Carolan; Jason E Gestwicki
Journal:  Bioorg Med Chem Lett       Date:  2011-03-01       Impact factor: 2.823

4.  Microwave-assisted synthesis of a 3-aminoimidazo[1,2-a]-pyridine/pyrazine library by fluorous multicomponent reactions and subsequent cross-coupling reactions.

Authors:  Yimin Lu; Wei Zhang
Journal:  QSAR Comb Sci       Date:  2004

5.  MCR synthesis of a tetracyclic tetrazole scaffold.

Authors:  Pravin Patil; Kareem Khoury; Eberhardt Herdtweck; Alexander Dömling
Journal:  Bioorg Med Chem       Date:  2014-12-20       Impact factor: 3.641

6.  Expanding the substrate scope of Ugi five-center, four-component reaction U-5C-4CR): ketones as coupling partners for secondary amino acids.

Authors:  Maciej Dawidowski; Sławomir Sobczak; Marcin Wilczek; Artur Kulesza; Jadwiga Turło
Journal:  Mol Divers       Date:  2013-10-24       Impact factor: 2.943

7.  Concise Synthesis of Macrocycles by Multicomponent Reactions.

Authors:  Eman M M Abdelraheem; Samad Khaksar; Alexander Dömling
Journal:  Synthesis (Stuttg)       Date:  2018-01-10       Impact factor: 3.157

Review 8.  Groebke-Blackburn-Bienaymé multicomponent reaction: emerging chemistry for drug discovery.

Authors:  Saad Shaaban; Bakr F Abdel-Wahab
Journal:  Mol Divers       Date:  2015-05-28       Impact factor: 2.943

9.  Convenient one-step synthesis of a medicinally relevant benzopyranopyridine system.

Authors:  Nikolai M Evdokimov; Artem S Kireev; Andrey A Yakovenko; Mikhail Yu Antipin; Igor V Magedov; Alexander Kornienko
Journal:  Tetrahedron Lett       Date:  2006-12-25       Impact factor: 2.415

10.  A novel synthesis of highly substituted imidazo[1,5-a]pyrazine derivatives by 3-CR/2-CR sequence.

Authors:  Ahmad Shaabani; Ali Maleki; Hamid Mofakham
Journal:  Mol Divers       Date:  2008-11-21       Impact factor: 2.943

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