Stereospecific Synthesis of (±)-1,2-Anhydro Methyl Rocaglate

2005-09-01T00:00:00Z (GMT) by Philip Magnus Matthew A. H. Stent
The rocaglates and analogues thereof have recently become targets for synthesis because of their potent antitumor activity. One of the major difficulties has been the control of stereochemistry of the adjacent −Ph and −An groups. In this letter we show that <b>14</b> is converted into <b>5</b> as a single stereoisomer and subsequently transformed into 1,2-anhydro methyl rocaglate <b>20</b>.