Literature DB >> 19590767

Creative approaches towards the synthesis of 2,5-dihydro- furans, thiophenes, and pyrroles. One method does not fit all!

Matthew Brichacek1, Jón T Njardarson.   

Abstract

A single method is never sufficient, which is why there is a great need for developing many diverse and creative approaches towards every chemical substrate class. This statement is supported by the contents of this perspective in addition to providing the reader with a helpful synthetic roadmap for selecting a suitable method for the building blocks being discussed. Detailed in this review are eight different synthetic approaches that provide access to valuable 2,5-dihydro- furan, thiophene and pyrrole building blocks. Each approach is briefly presented and its limits discussed. The strengths and weaknesses of each approach are further highlighted with a graphical table summary at the end. This summary clearly drives home the point that for every chemical substrate class we need many good methods in order to provide access to every member of each class.

Entities:  

Year:  2009        PMID: 19590767     DOI: 10.1039/b900236g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  5 in total

1.  Copper-Catalyzed Aminothiolation of 1,3-Dienes via a Dihydrothiazine Intermediate.

Authors:  Christopher E Sleet; Uttam K Tambar
Journal:  Angew Chem Int Ed Engl       Date:  2017-04-13       Impact factor: 15.336

2.  Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides.

Authors:  John M Motto; Alvaro Castillo; Alexander Greer; Laura K Montemayer; Erin E Sheepwash; Adrian L Schwan
Journal:  Tetrahedron       Date:  2011-02-04       Impact factor: 2.457

3.  Rhodium-catalyzed ring expansion of cyclopropanes to seven-membered rings by 1,5 C-C bond migration.

Authors:  Xiaoxun Li; Min Zhang; Dongxu Shu; Patrick J Robichaux; Suyu Huang; Weiping Tang
Journal:  Angew Chem Int Ed Engl       Date:  2011-09-09       Impact factor: 15.336

4.  Stereospecific ring expansion of chiral vinyl aziridines.

Authors:  Matthew Brichacek; Mauricio Navarro Villalobos; Alexandra Plichta; Jon T Njardarson
Journal:  Org Lett       Date:  2011-02-10       Impact factor: 6.005

5.  Synthesis, Spectral Analysis, In Vitro Microbiological Evaluation, and Molecular Docking Studies of Some Novel 1-(1-Aryl-1H-tetrazol-5-yl)-2-(piperidin-1-yl)ethanone Derivatives.

Authors:  Thangasamy Elavarasan; Durairaj Peter Bhakiaraj; Mannathusamy Gopalakrishnan
Journal:  ISRN Org Chem       Date:  2014-05-06
  5 in total

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