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Efficient assembly of threaded molecular machines for sequence-specific synthesis.
De Bo, Guillaume; Kuschel, Sonja; Leigh, David A; Lewandowski, Bartosz; Papmeyer, Marcus; Ward, John W.
Afiliação
  • De Bo G; School of Chemistry, University of Manchester , Oxford Road, Manchester, M13 9PL United Kingdom.
J Am Chem Soc ; 136(15): 5811-4, 2014 Apr 16.
Article em En | MEDLINE | ID: mdl-24678971
ABSTRACT
We report on an improved strategy for the preparation of artificial molecular machines that can pick up and assemble reactive groups in sequence by traveling along a track. In the new approach a preformed rotaxane synthon is attached to the end of an otherwise fully formed strand of building blocks. This "rotaxane-capping" protocol is significantly more efficient than the "final-step-threading" method employed previously and enables the synthesis of threaded molecular machines that operate on extended oligomer, and potentially polymer, tracks. The methodology is exemplified through the preparation of a machine that adds four amino acid building blocks from a strand in sequence, featuring up to 20-membered ring native chemical ligation transition states.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rotaxanos Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rotaxanos Idioma: En Ano de publicação: 2014 Tipo de documento: Article