Literature DB >> 18421381

The synthesis of enantiomerically pure [2.2]paracyclophane derivatives.

Gareth J Rowlands1.   

Abstract

[2.2]Paracyclophane is a fascinating molecule that offers great potential in a wide range of chemical disciplines. Currently, the synthesis of the majority of enantiomerically pure [2.2]paracyclophane derivatives is based on the resolution of a small number of starting materials or individual resolution procedures are developed for each new compound. The development of more general routes to these valuable compounds via the resolution of a common intermediate is discussed. Ultimately, it would be preferable to synthesise these valuable compounds without recourse to resolution and ideas for this rewarding goal are postulated.

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Year:  2008        PMID: 18421381     DOI: 10.1039/b800698a

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


  4 in total

1.  5,8-Dibromo-15,18-dimeth-oxy-2,11-dithia-[3.3]paracyclo-phane.

Authors:  Guojun Jin; Yinghui Lu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-07-31

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.  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

  4 in total

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