Literature DB >> 16100609

The synthesis of enantiomerically pure 4-substituted [2.2]paracyclophane derivatives by sulfoxide-metal exchange.

Peter B Hitchcock1, Gareth J Rowlands, Rakesh Parmar.   

Abstract

A general strategy for the synthesis of enantiomerically pure 4-substituted [2.2]paracyclophanes from a common sulfoxide precursor is described.

Entities:  

Year:  2005        PMID： 16100609     DOI： 10.1039/b507394d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  5 in total

Review 1.  Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives.

Authors:  Zahid Hassan; Eduard Spuling; Daniel M Knoll; Stefan Bräse
Journal:  Angew Chem Int Ed Engl       Date:  2019-10-30       Impact factor: 15.336

2.  Chiral isothiourea-catalyzed kinetic resolution of 4-hydroxy[2.2]paracyclophane.

Authors:  David Weinzierl; Mario Waser
Journal:  Beilstein J Org Chem       Date:  2021-04-08       Impact factor: 2.883

3.  The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C-H activation.

Authors:  Shashank Tewari; Maulik N Mungalpara; Suraj Patel; Gareth J Rowlands
Journal:  RSC Adv       Date:  2022-03-17       Impact factor: 3.361

4.  Synthesis of a Ni Complex Chelated by a [2.2]Paracyclophane-Functionalized Diimine Ligand and Its Catalytic Activity for Olefin Oligomerization.

Authors:  Daisuke Takeuchi; Yoshi-Aki Tojo; Kohtaro Osakada
Journal:  Molecules       Date:  2021-05-05       Impact factor: 4.411

5.  Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives.

Authors:  Gareth J Rowlands; Richard J Seacome
Journal:  Beilstein J Org Chem       Date:  2009-03-12       Impact factor: 2.883
  5 in total

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