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Chemoenzymatic synthesis of chiral 4,4 '-bipyridyls and their metal-organic frameworks

Lookup NU author(s): Emeritus Professor Bill CleggORCiD, Dr Ross Harrington

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Abstract

The first enantiopure 4,4'-bipyridyls, 6, 8, and 9 have been prepared in four or five steps via bacterial dioxygenase-catalysed cis-dihydroxylation of 4-chloroquinoline 1 and C-C coupling; ligands 6 and 9 are found to be effective building blocks for the preparation of chiral metal-organic frameworks as demonstrated with the rational synthesis of two pillared-grid structures [Zn-2(fumarate)(2)(L)], which exhibit interesting structural and dynamic aspects.

Publication metadata

Author(s): Sbircea L, Sharma ND, Clegg W, Harrington RW, Horton PN, Hursthouse MB, Apperley DC, Boyd DR, James SL

Publication type: Article

Publication status: Published

Journal: Chemical Communications

Year: 2008

Issue: 43

Pages: 5538-5540

Print publication date: 01/01/2008

ISSN (print): 1359-7345

ISSN (electronic): 1364-548X

Publisher: Royal Society of Chemistry

URL: http://dx.doi.org/10.1039/b812366g

DOI: 10.1039/b812366g

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