Regio- and stereoselectivity of spirodienone formation in 2,14-dithiacalix[4]arene

Author:

Kortus D.12345,Eigner V.6745,Lhoták P.12345ORCID

Affiliation:

1. Department of Organic Chemistry

2. University of Chemistry and Technology

3. Prague (UCTP)

4. 166 28 Prague 6

5. Czech Republic

6. Department of Solid State Chemistry

7. UCTP

Abstract

Within the mixed-bridge system the thiacalixarene fragment (Ar–S–Ar) is much more prone to spirocyclization than the calixarene one (Ar–CH2–Ar).

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Grantová Agentura České Republiky

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Reference46 articles.

1. Calixarenes and Beyond , ed. P. Neri , J. L. Sessler and M. X. Wang , Springer , Cham, Switzerland , 2016

2. C. D. Gutsche , Calixarenes: An Introduction , Royal Society of Chemistry , Cambridge, UK , 2nd edn, 2008

3. Calixarenes in the Nanoworld , ed. J. Vicens , J. Harrowfield and L. Backlouti , Springer , Dordrecht, The Netherlands , 2007

4. Calixarenes 2001 , ed. Z. Asfari , V. Böhmer , J. Harrowfield and J. Vicens , Kluwer , Dordrecht, The Netherlands , 2001

5. Calixarenes in Action , ed. L. Mandolini and R. Ungaro , Imperial College Press , London , 2000

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