Literature DB >> 31983781

Recent advances in the application of ring-closing metathesis for the synthesis of unsaturated nitrogen heterocycles.

Emilia J Groso1, Corinna S Schindler1.   

Abstract

This short review summarizes recent advances relating to the application of ring-closing olefin-olefin and carbonyl-olefin metathesis reactions towards the synthesis of unsaturated five- and six-membered nitrogen heterocycles. These developments include catalyst modifications and reaction designs that will enable access to more complex nitrogen heterocycles.

Entities:  

Keywords:  Lewis acid catalysis; RCM; carbonyl-olefin metathesis; catalyst design; nitrogen heterocycles; ruthenium

Year:  2019        PMID： 31983781      PMCID： PMC6983305          DOI： 10.1055/s-0037-1611651

Source DB:  PubMed          Journal:  Synthesis (Stuttg)        ISSN： 0039-7881            Impact factor:   3.157


  94 in total

1.  A practical and highly active ruthenium-based catalyst that effects the cross metathesis of acrylonitrile.

Authors:  Jennifer A Love; John P Morgan; Tina M Trnka; Robert H Grubbs
Journal:  Angew Chem Int Ed Engl       Date:  2002-11-04       Impact factor: 15.336

2.  A catalytic approach to (R)-(+)-muscopyridine with integrated "self-clearance".

Authors:  Alois Fürstner; Andreas Leitner
Journal:  Angew Chem Int Ed Engl       Date:  2003-01-20       Impact factor: 15.336

3.  Ruthenium-catalyzed cyclizations: more than just olefin metathesis!

Authors:  Bernd Schmidt
Journal:  Angew Chem Int Ed Engl       Date:  2003-10-27       Impact factor: 15.336

4.  Studies on electronic effects in O-, N- and S-chelated ruthenium olefin-metathesis catalysts.

Authors:  Eyal Tzur; Anna Szadkowska; Amos Ben-Asuly; Anna Makal; Israel Goldberg; Krzysztof Woźniak; Karol Grela; N Gabriel Lemcoff
Journal:  Chemistry       Date:  2010-08-02       Impact factor: 5.236

5.  Amine-promoted asymmetric (4+2) annulations for the enantioselective synthesis of tetrahydropyridines: a traceless and recoverable auxiliary strategy.

Authors:  Pengfei Hu; Jian Hu; Jiajun Jiao; Xiaofeng Tong
Journal:  Angew Chem Int Ed Engl       Date:  2013-04-09       Impact factor: 15.336

6.  The pivotal role of symmetry in the ruthenium-catalyzed ring-closing metathesis of olefins.

Authors:  Chiara Costabile; Annaluisa Mariconda; Luigi Cavallo; Pasquale Longo; Valerio Bertolasi; Francesco Ragone; Fabia Grisi
Journal:  Chemistry       Date:  2011-06-15       Impact factor: 5.236

7.  Efficient ring-closing metathesis of alkenyl bromides: the importance of protecting the catalyst during the olefin approach.

Authors:  Michele Gatti; Emma Drinkel; Linglin Wu; Ivano Pusterla; Fiona Gaggia; Reto Dorta
Journal:  J Am Chem Soc       Date:  2010-11-03       Impact factor: 15.419

8.  Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.

Authors:  Bodo Scheiper; Frank Glorius; Andreas Leitner; Alois Fürstner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-12       Impact factor: 11.205

9.  Predicting the cis-trans dichloro configuration of group 15-16 chelated ruthenium olefin metathesis complexes: a DFT and experimental study.

Authors:  Charles E Diesendruck; Eyal Tzur; Amos Ben-Asuly; Israel Goldberg; Bernd F Straub; N Gabriel Lemcoff
Journal:  Inorg Chem       Date:  2009-11-16       Impact factor: 5.165

10.  Insights into the decomposition of olefin metathesis precatalysts.

Authors:  Simone Manzini; Albert Poater; David J Nelson; Luigi Cavallo; Alexandra M Z Slawin; Steven P Nolan
Journal:  Angew Chem Int Ed Engl       Date:  2014-06-02       Impact factor: 15.336
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  2 in total

1.  Synthesis of 2H-Chromenes via Hydrazine-Catalyzed Ring-Closing Carbonyl-Olefin Metathesis.

Authors:  Yunfei Zhang; Janis Jermaks; Samantha N MacMillan; Tristan H Lambert
Journal:  ACS Catal       Date:  2019-09-10       Impact factor: 13.084

Review 2.  Carbonyl-Olefin Metathesis.

Authors:  Haley Albright; Ashlee J Davis; Jessica L Gomez-Lopez; Hannah L Vonesh; Phong K Quach; Tristan H Lambert; Corinna S Schindler
Journal:  Chem Rev       Date:  2021-06-16       Impact factor: 72.087
  2 in total

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