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Interdependent Dynamic Nitroaldol and Boronic Ester Reactions for Complex Dynamers of Different Topologies.
Karalius, Antanas; Qi, Yunchuan; Ayinla, Mubarak; Szabó, Zoltán; Ramström, Olof.
Affiliation
  • Karalius A; KTH Royal Institute of Technology, Chemistry, Teknikringen 36, S-10044, Stockholm, SWEDEN.
  • Qi Y; University of Massachusetts Lowell, Chemistry, One University Ave., 01854, Lowell, UNITED STATES OF AMERICA.
  • Ayinla M; University of Massachusetts Lowell, Chemistry, One University Ave., 01854, Lowell, UNITED STATES OF AMERICA.
  • Szabó Z; KTH Royal Institute of Technology, Chemistry, Teknikringen 36, S-10044, Stockholm, SWEDEN.
  • Ramström O; Royal Institute of Technology, Department of Chemistry, Teknikringen 30, 10044, Stockholm, SWEDEN.
Chemistry ; : e202402409, 2024 Aug 25.
Article in En | MEDLINE | ID: mdl-39183180
ABSTRACT
Complex dynamic systems displaying interdependency between nitroaldol and boronic ester reactions have been demonstrated. Nitroalkane-1,3-diols, generated by the nitroaldol reaction, were susceptible to ester formation with different boronic acids in aprotic solvents, whereas hydrolysis of the esters occurred in the presence of water. The boronic ester formation led to significant stabilization of the nitroaldol adducts under basic conditions. The use of bifunctional building blocks was furthermore established, allowing for main chain nitroaldol-boronate dynamers as well as complex network dynamers with distinct topologies. The shape and rigidity of the resulting dynamers showed an apparent dependency on the configuration of the boronic acids.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Sweden Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Sweden Country of publication: Germany