Synthesis of a new class of 5′-functionalized adenosines using a Rh(II)-catalyzed 1,3-dipolar cycloaddition

Fei Liu, David J. Austin*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Citations (Scopus)

Abstract

(matrix presented) Chemically protected adenosine was functionalized at the 5′ position to generate novel dipolarophiles and mesoionic dipoles. These species were found to undergo facile 1,3-dipolar cycloaddition to afford a new series of adenosine derivatives that contain a point of diversification at the 5′ position of adenosine.

Original languageEnglish
Pages (from-to)2273-2276
Number of pages4
JournalOrganic Letters
Volume3
Issue number15
DOIs
Publication statusPublished - 26 Jul 2001
Externally publishedYes

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