Literature DB >> 12298030

Triazenes: a versatile tool in organic synthesis.

David B Kimball1, Michael M Haley.   

Abstract

Triazenes (RN=N-NR'R") are a class of compounds that hold much promise in preparative chemistry as they are reactive groups which are both stable and adaptable to numerous synthetic transformations. Useful to scientists in pharmacology, total synthesis, polymer technology, and the construction of novel ring systems, to name a few areas, triazenes also have a tendency to surprise chemists with new reactions and increasing applicability. This review highlights some of the recent advances and diversity possible with these types of systems.

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Year:  2002        PMID: 12298030     DOI: 10.1002/1521-3773(20020916)41:18<3338::AID-ANIE3338>3.0.CO;2-7

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  13 in total

1.  Selective Protection of Secondary Amines as the N-Phenyltriazenes. Application to Aminoglycoside Antibiotics.

Authors:  Amr Sonousi; David Crich
Journal:  Org Lett       Date:  2015-08-04       Impact factor: 6.005

2.  Binuclear palladium(I) and palladium(II) complexes of ortho-functionalized 1,3-bis(aryl)triazenido ligands.

Authors:  Juan José Nuricumbo-Escobar; Carlos Campos-Alvarado; Gustavo Ríos-Moreno; David Morales-Morales; Patrick J Walsh; Miguel Parra-Hake
Journal:  Inorg Chem       Date:  2007-06-20       Impact factor: 5.165

3.  Polymer nanofibre junctions of attolitre volume serve as zeptomole-scale chemical reactors.

Authors:  Pavel Anzenbacher; Manuel A Palacios
Journal:  Nat Chem       Date:  2009-03-08       Impact factor: 24.427

4.  G2, G3, and complete basis set calculations of the thermodynamic properties of cis- and trans-triazene.

Authors:  Ryan M Richard; David W Ball
Journal:  J Mol Model       Date:  2007-10-23       Impact factor: 1.810

5.  Use of hydroxylamines, hydroxamic acids, oximes and amines as nucleophiles in the Zbiral oxidative deamination of N-acetyl neuraminic acid. Isolation and characterization of novel mono- and disubstitution products.

Authors:  Mohammed Hawsawi; Michael G Pirrone; Anura Wickramasinghe; David Crich
Journal:  Carbohydr Res       Date:  2020-01-25       Impact factor: 2.104

6.  A phosphine-mediated conversion of azides into diazo compounds.

Authors:  Eddie L Myers; Ronald T Raines
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

7.  Guided desaturation of unactivated aliphatics.

Authors:  Ana-Florina Voica; Abraham Mendoza; Will R Gutekunst; Jorge Otero Fraga; Phil S Baran
Journal:  Nat Chem       Date:  2012-07-08       Impact factor: 24.427

8.  Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes.

Authors:  Sangwon Seo; Ming Gao; Eva Paffenholz; Michael C Willis
Journal:  ACS Catal       Date:  2021-05-05       Impact factor: 13.084

9.  A triazine-based BODIPY trimer as a molecular viscometer.

Authors:  Sangram L Raut; Joseph D Kimball; Rafal Fudala; Ilkay Bora; Rahul Chib; Hana Jaafari; Marlius K Castillo; Nicholas W Smith; Ignacy Gryczynski; Sergei V Dzyuba; Zygmunt Gryczynski
Journal:  Phys Chem Chem Phys       Date:  2016-02-14       Impact factor: 3.676

10.  Transition metal-free intramolecular regioselective couplings of aliphatic and aromatic C-H bonds.

Authors:  Hua Tian; Haijun Yang; Changjin Zhu; Hua Fu
Journal:  Sci Rep       Date:  2016-01-29       Impact factor: 4.379

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