Sutton L, Donaubauer W, Hampel F, Hirsch A (2004)
Publication Type: Journal article, Original article
Publication year: 2004
Original Authors: Sutton L.R., Donaubauer W.A., Hampel F., Hirsch A.
Publisher: Royal Society of Chemistry
Book Volume: 10
Pages Range: 1758-1759
Journal Issue: 15
DOI: 10.1039/b401021c
Mixtures of isomers are available from the reaction of benzene hexathiol with three equivalents of p-tolualdehyde and kinetic traps avoided under the reported catalytic conditions, establishing tris(thioacetals) as potential building blocks for covalently self-assembled complex structures.
APA:
Sutton, L., Donaubauer, W., Hampel, F., & Hirsch, A. (2004). Tris(thioacetals) from benzene hexathiol: Towards covalent self-assembly. Chemical Communications, 10(15), 1758-1759. https://doi.org/10.1039/b401021c
MLA:
Sutton, Liam, et al. "Tris(thioacetals) from benzene hexathiol: Towards covalent self-assembly." Chemical Communications 10.15 (2004): 1758-1759.
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