General, Divergent Platform for Diastereoselective Synthesis of trans-Cyclooctenes with High Reactivity and Favorable Physiochemical Properties*.

Pigga, Jessica E; Rosenberger, Julia E; Jemas, Andrew; Boyd, Samantha J; Dmitrenko, Olga; Xie, Yixin; Fox, Joseph M

Pigga, Jessica E; Rosenberger, Julia E; Jemas, Andrew; Boyd, Samantha J; Dmitrenko, Olga; Xie, Yixin; Fox, Joseph M.

Afiliação

Pigga JE; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Rosenberger JE; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Jemas A; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Boyd SJ; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Dmitrenko O; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Xie Y; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.
Fox JM; Department of Chemistry and Biochemistry, University of Delaware, 163 The Green, Newark, DE, 19716, USA.

Angew Chem Int Ed Engl ; 60(27): 14975-14980, 2021 06 25.

Article em En | MEDLINE | ID: mdl-33742526

Assuntos

Ciclo-Octanos/síntese química; Físico-Química; Reação de Cicloadição; Ciclo-Octanos/química; Células HeLa; Humanos; Estrutura Molecular; Estereoisomerismo

Palavras-chave

biorthogonal reactions; diastereoselectivity; synthetic methods; tetrazines; trans-cyclooctenes

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ciclo-Octanos Limite: Humans Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

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