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P(V) Reagents for the Scalable Synthesis of Natural and Modified Nucleoside Triphosphates.
Liao, Jen-Yu; Bala, Saikat; Ngor, Arlene K; Yik, Eric J; Chaput, John C.
Afiliación
  • Liao JY; Departments of Pharmaceutical Sciences, Chemistry, and Molecular Biology and Biochemistry , University of California , Irvine , California 92697-3958 , United States.
  • Bala S; Departments of Pharmaceutical Sciences, Chemistry, and Molecular Biology and Biochemistry , University of California , Irvine , California 92697-3958 , United States.
  • Ngor AK; Departments of Pharmaceutical Sciences, Chemistry, and Molecular Biology and Biochemistry , University of California , Irvine , California 92697-3958 , United States.
  • Yik EJ; Departments of Pharmaceutical Sciences, Chemistry, and Molecular Biology and Biochemistry , University of California , Irvine , California 92697-3958 , United States.
  • Chaput JC; Departments of Pharmaceutical Sciences, Chemistry, and Molecular Biology and Biochemistry , University of California , Irvine , California 92697-3958 , United States.
J Am Chem Soc ; 141(34): 13286-13289, 2019 08 28.
Article en En | MEDLINE | ID: mdl-31298849
ABSTRACT
Natural and modified nucleoside triphosphates impact nearly every major aspect of healthcare research from DNA sequencing to drug discovery. However, a scalable synthetic route to these molecules has long been hindered by the need for purification by high performance liquid chromatography (HPLC). Here, we describe a fundamentally different approach that uses a novel P(V) pyrene pyrophosphate reagent to generate derivatives that are purified by silica gel chromatography and converted to the desired compounds on scales vastly exceeding those achievable by HPLC. The power of this approach is demonstrated through the synthesis of a broad range of natural and unnatural nucleoside triphosphates (dNTPs and xNTPs) using protocols that are efficient, inexpensive, and operationally straightforward.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Nucleótidos Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Nucleótidos Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article