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Benhaim C.,Janssen Chemical Development | Lemaire S.,Janssen Chemical Development | Gaekens T.,Janssen Chemical Development | Govaerts T.,Janssen Chemical Development | And 8 more authors.

The synthesis of an anti-infective nucleoside intermediate was accomplished through direct iodine displacement at C-5′ by a tetrabutylammonium carboxylate. This approach constitutes a more efficient alternative to the traditional oxidative displacement. © Georg Thieme Verlag Stuttgart New York. Source

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