LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Synthesis of N6‐Substituted Adenosines as Cytokinin Nucleosides

Photo by impulsq from unsplash

This unit describes preparation of N6‐substituted adenosines (cytokinin nucleosides), a unique class of compounds with a wide spectrum of biological activities. Regioselective alkylation of N6‐acetyl‐2′,3′,5′‐tri‐O‐acetyladenosine with alkyl halides under basic… Click to show full abstract

This unit describes preparation of N6‐substituted adenosines (cytokinin nucleosides), a unique class of compounds with a wide spectrum of biological activities. Regioselective alkylation of N6‐acetyl‐2′,3′,5′‐tri‐O‐acetyladenosine with alkyl halides under basic conditions or alcohols under Mitsunobu conditions followed by deprotection are the methods of choice for the preparation of the cytokinin nucleosides. The attractive feature of this strategy is the possibility of using a broad library of commercially available alkyl halides and alcohols under mild reaction conditions. © 2018 by John Wiley & Sons, Inc.

Keywords: cytokinin; substituted adenosines; chemistry; synthesis substituted; cytokinin nucleosides; adenosines cytokinin

Journal Title: Current Protocols in Nucleic Acid Chemistry
Year Published: 2018

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.