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This fully protected compound, <jats:bold>3<\/jats:bold>, was submitted to a <jats:italic>Mitsunobu<\/jats:italic> reaction with the <jats:italic>N<\/jats:italic>\u2010hydroxysuccinimide (NHS) ester, <jats:bold>5<\/jats:bold>, of (2<jats:italic>E<\/jats:italic>)\u201010\u2010hydroxydec\u20102\u2010enoic acid (<jats:bold>4<\/jats:bold>) which gave nucleolipid <jats:bold>6<\/jats:bold>. The latter was detritylated with Cl<jats:sub>2<\/jats:sub>CHCOOH to yield the co\u2010drug <jats:bold>7<\/jats:bold> as NHS ester.<\/jats:p>","DOI":"10.1002\/cbdv.201500048","type":"journal-article","created":{"date-parts":[[2015,9,13]],"date-time":"2015-09-13T16:36:34Z","timestamp":1442162194000},"page":"1307-1312","source":"Crossref","is-referenced-by-count":2,"title":["<i>Mitsunobu<\/i> Alkylation of Cancerostatic 5\u2010Fluorouridine with (2<i>E<\/i>)\u201010\u2010Hydroxydec\u20102\u2010enoic Acid, a Fatty Acid from Royal Jelly with Multiple Biological Activities"],"prefix":"10.1002","volume":"12","author":[{"given":"Vanessa","family":"Ottenhaus","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Helmut","family":"Rosemeyer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2015,9,13]]},"reference":[{"key":"e_1_2_1_1_2","unstructured":"D.Steinhilber M.Schubert\u2010Zsilavecz H. 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