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An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations

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UNSPECIFIED (2005) An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations. ORGANIC & BIOMOLECULAR CHEMISTRY, 3 (10). pp. 1880-1892. ISSN 1477-0520.

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Abstract

Bromine has been added to cis, trans, trans-1,5,9-cyclododecatriene under various reaction conditions. All expected direct addition products have been isolated, and their structures have been determined by microanalysis, NMR and X-ray crystallography. Advanced NMR techniques were used to determine solution conformations of several of the compounds, enabling comparison with the solid-state conformations obtained by crystallography.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: ORGANIC & BIOMOLECULAR CHEMISTRY
Publisher: ROYAL SOC CHEMISTRY
ISSN: 1477-0520
Official Date: 2005
Dates:
DateEvent
2005UNSPECIFIED
Volume: 3
Number: 10
Number of Pages: 13
Page Range: pp. 1880-1892
Publication Status: Published

Data sourced from Thomson Reuters' Web of Knowledge

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