Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224476 | Tetrahedron | 2008 | 6 Pages |
Abstract
With an aim to synthesize 4â²-substituted cordycepins, the 4â²-benzoyloxy precursor (9) was prepared from adenosine through an electrophilic addition (iodo-benzoyloxylation) to the 4â²,5â²-unsaturated derivative (5) and subsequent radical-mediated removal of the 3â²-iodine atom of the resulting adducts (6). Usefulness of 9 was briefly verified by synthesizing the 4â²-allyl (12) and 4â²-cyano (13) analogues of cordycepin.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yutaka Kubota, Mayumi Kunikata, Nobuhide Ishizaki, Kazuhiro Haraguchi, Yuki Odanaka, Hiromichi Tanaka,