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http://dx.doi.org/10.1002/anie.201001625 | DOI Listing |
Angew Chem Int Ed Engl
February 2024
Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
The solvent and catalyst free thermolysis of biphenylenes at 350 °C furnishes [n]cyclo-ortho-phenylenes ([n]COPs, n=4-10) in one step and in high yields. At 400 °C biphenylene dimerizes into tetraphenylene, but lower reaction temperatures produce cyclooligomers. If suitably substituted, the oligomers are soluble and can be isolated and characterized.
View Article and Find Full Text PDFOrg Lett
April 2019
School of Biological Sciences , Nanyang Technological University, 60 Nanyang Drive , Singapore 637551.
A biomimetic one-step ligase-catalyzed cyclo-oligomerization mediated by butelase 1, an Asn/Asp-specific ligase, is introduced that is time-, concentration-, length-, and sequence-dependent. This reaction yields cyclic mono-, di-, tri-, and tetramers from peptide precursors containing 3-15 amino acids ended with Asn and a His-Val tail. The cyclomonomers were favored when the peptide lengths were >9 amino acids.
View Article and Find Full Text PDFJ Am Chem Soc
June 2012
Department of Chemistry, University of Illinois at Urbana-Champaign, 61801, United States.
Macrocyclic oligomers possessing direction-defining ester linkages were synthesized via metathesis of the nondirectional alkyne functional group. Alkyne metathesis is expected to scramble the relative orientation of adjacent ester groups, potentially leading to a complex mixture of macrocyclic products. We wondered whether a narrow product distribution would be achievable with a proper choice of the building block structure.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2010
Kekulé-Institut für Organische Chemie und Biochemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Strasse 1, 53121 Bonn, Germany.
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