Literature DB >> 22081884

Synthesis of aziridines from alkenes and aryl azides with a reusable macrocyclic tetracarbene iron catalyst.

S Alan Cramer1, David M Jenkins.   

Abstract

A new iron aziridination catalyst supported by a macrocyclic tetracarbene ligand has been synthesized. The catalyst, [((Me,Et)TC(Ph))Fe(NCCH(3))(2)](PF(6))(2), was synthesized from the tetraimidazolium precursor ((Me,Et)TC(Ph))(I)(4) and characterized by NMR spectroscopy, electrospray ionization mass spectrometry, and single-crystal X-ray diffraction. This iron complex catalyzes the aziridination of electron-donating aryl azides and a wide variety of substituted aliphatic alkenes, including tetrasubstituted ones, in a "C(2) + N(1)" addition reaction. Finally, the catalyst can be recovered and reused up to three additional times without significant reduction in yield.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 22081884     DOI: 10.1021/ja2090965

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  23 in total

1.  Oxidative nitrene transfer from azides to alkynes via Ti(ii)/Ti(iv) redox catalysis: formal [2+2+1] synthesis of pyrroles.

Authors:  Adam J Pearce; Xin Yi See; Ian A Tonks
Journal:  Chem Commun (Camb)       Date:  2018-06-19       Impact factor: 6.222

2.  Arene C-H amination at nickel in terphenyl-diphosphine complexes with labile metal-arene interactions.

Authors:  David E Herbert; Nadia C Lara; Theodor Agapie
Journal:  Chemistry       Date:  2013-10-14       Impact factor: 5.236

3.  Styrene Aziridination by Iron(IV) Nitrides.

Authors:  Salvador B Muñoz; Wei-Tsung Lee; Diane A Dickie; Jeremiah J Scepaniak; Deepak Subedi; Maren Pink; Michael D Johnson; Jeremy M Smith
Journal:  Angew Chem Int Ed Engl       Date:  2015-07-15       Impact factor: 15.336

4.  Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins.

Authors:  Honghui Lei; Tomislav Rovis
Journal:  J Am Chem Soc       Date:  2019-02-04       Impact factor: 15.419

5.  Elucidation of the Reaction Mechanism of C2 + N1 Aziridination from Tetracarbene Iron Catalysts.

Authors:  Sara B Isbill; Preeti P Chandrachud; Jesse L Kern; David M Jenkins; Sharani Roy
Journal:  ACS Catal       Date:  2019-05-31       Impact factor: 13.084

6.  Unprecedented Five-Coordinate Iron(IV) Imides Generate Divergent Spin States Based on the Imide R-Groups.

Authors:  Markus R Anneser; Gaya R Elpitiya; Jacob Townsend; Elizabeth J Johnson; Xian B Powers; Joseph F DeJesus; Konstantinos D Vogiatzis; David M Jenkins
Journal:  Angew Chem Int Ed Engl       Date:  2019-05-07       Impact factor: 15.336

7.  Catalytic aziridination with alcoholic substrates via a chromium tetracarbene catalyst.

Authors:  C Luke Keller; Jesse L Kern; Bradley D Terry; Sharani Roy; David M Jenkins
Journal:  Chem Commun (Camb)       Date:  2018-01-04       Impact factor: 6.222

8.  Room Temperature Activation of Aryloxysulfonyl Azides by [Co(II)(TPP)] for Selective Radical Aziridination of Alkenes via Metalloradical Catalysis.

Authors:  Velusamy Subbarayan; Li-Mei Jin; Cui Xin; X Peter Zhang
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

9.  Inverting Steric Effects: Using "Attractive" Noncovalent Interactions To Direct Silver-Catalyzed Nitrene Transfer.

Authors:  Minxue Huang; Tzuhsiung Yang; Jonathan D Paretsky; John F Berry; Jennifer M Schomaker
Journal:  J Am Chem Soc       Date:  2017-11-20       Impact factor: 15.419

10.  Effective synthesis of chiral N-fluoroaryl aziridines through enantioselective aziridination of alkenes with fluoroaryl azides.

Authors:  Li-Mei Jin; Xue Xu; Hongjian Lu; Xin Cui; Lukasz Wojtas; X Peter Zhang
Journal:  Angew Chem Int Ed Engl       Date:  2013-04-15       Impact factor: 15.336

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