Literature DB >> 17406624

The use of the Ugi four-component condensation.

Stefano Marcaccini1, Tomás Torroba.   

Abstract

This protocol describes a procedure for the Ugi four-component condensation. It describes the general mechanism as well as the effects of the nature of the components on the Ugi reaction. It also describes the effects of the reaction conditions on the reaction, along with special procedures and workup. The experimental procedure is exemplified by a description of the preparation of N-cyclohexyl 2-[N-(2-chloroacetyl)-N-(4-chlorobenzyl)]amino-2-(4-chlorophenyl)acetamide, a typical Ugi product, that is subsequently used for the synthesis of a 2,5-diketopiperazine, an example of an important type of pharmaceutical compound. The experimental procedure is then extended to the synthesis of a 1,5-disubstituted tetrazole via Ugi four-component condensation. The protocol describes the preparation and characterization of the new 1-cyclohexyl-5-(1-phenylamino-2-methyl)propyltetrazole. The total time for the synthesis and isolation of the two example reactions in parallel is 3 d.

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Year:  2007        PMID: 17406624     DOI: 10.1038/nprot.2007.71

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  30 in total

1.  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

2.  Synthesis of peptide macrocycles using unprotected amino aldehydes.

Authors:  Benjamin H Rotstein; Vishal Rai; Ryan Hili; Andrei K Yudin
Journal:  Nat Protoc       Date:  2010-10-21       Impact factor: 13.491

3.  Multicomponent synthesis of benzoxazinones via tandem Ugi/Mitsunobu reactions: an unexpected cine-substitution.

Authors:  Luca Banfi; Andrea Basso; Giuseppe Guanti; Paulina Lecinska; Renata Riva
Journal:  Mol Divers       Date:  2008-09-02       Impact factor: 2.943

4.  Solid-phase synthesis of N-substituted pyrrolidinone-tethered N-substituted piperidines via Ugi reaction.

Authors:  Zhang Liu; Adel Nefzi
Journal:  J Comb Chem       Date:  2010-07-12

5.  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

6.  Concise route to a series of novel 3-(tetrazol-5-yl)quinoxalin-2(1H)-ones.

Authors:  Steven Gunawan; Gary Nichol; Christopher Hulme
Journal:  Tetrahedron Lett       Date:  2012-01-28       Impact factor: 2.415

7.  Studies toward a library of tetrahydrofurans: click and MCR products of mono- and bis-tetrahydrofurans.

Authors:  Jitendra K Mishra; Peter Wipf; Subhash C Sinha
Journal:  J Comb Chem       Date:  2010-09-13

Review 8.  Tetrazoles via Multicomponent Reactions.

Authors:  Constantinos G Neochoritis; Ting Zhao; Alexander Dömling
Journal:  Chem Rev       Date:  2019-02-01       Impact factor: 60.622

9.  Aldol reactions in multicomponent reaction based domino pathways: a multipurpose enabling tool in heterocyclic chemistry.

Authors:  Zhigang Xu; Fabio De Moliner; Alexandra P Cappelli; Christopher Hulme
Journal:  Org Lett       Date:  2013-05-29       Impact factor: 6.005

10.  Optimization of the Ugi reaction using parallel synthesis and automated liquid handling.

Authors:  Jean-Claude Bradley; Khalid Baig Mirza; Tom Osborne; Antony Wiliams; Kevin Owens
Journal:  J Vis Exp       Date:  2008-11-11       Impact factor: 1.355

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