01177nas a2200229   4500008004100000022001400041245010100055210006900156260010600225300001200331490000700343520028100350653002000631653001600651653002100667653003200688653002800720100002800748700002400776700002300800856012400823       2009                        eng d  a0040-403900aHighly stereoselective approach toward the synthesis of the macrolactone core of amphidinolide W0 aHighly stereoselective approach toward the synthesis of the macr  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcFEB  a755-7580 v503 a<p>The diastereoselective synthesis of the macrolactone core of amphidinolide W was successfully accomplished using Evans' asymmetric alkylation, Aldol reaction, Julia-Kocienski olefination, and Kita's macrocyclization protocol. (C) 2008 Elsevier Ltd. All rights reserved.</p>10aAmphidinolide W10aEvans aldol10aEvans alkylation10aJulia-Kocienski olefination10aKita's macrocyclization1 aMohapatra, Debendra, K.1 aChatterjee, Bhaskar1 aGurjar, Mukund, K.  uhttps://library.ncl.res.in/content/highly-stereoselective-approach-toward-synthesis-macrolactone-core-amphidinolide-w-0