01440nas a2200241   4500008004100000022001400041245017500055210006900230260007500299300001400374490000700388520045500395653002000850653002500870653002300895653005000918653002500968653002100993653001401014100002301028700001901051856012801070       2016                        eng d  a0039-788100aChemoenzymatic access to (+)-artabotriol and its application in collective synthesis of (+)-grandiamide D, (-)-tulipalin B, (+)-spirathundiol, and (+)-artabotriolcaffeate0 aChemoenzymatic access to artabotriol and its application in coll  aRUDIGERSTR 14, D-70469 STUTTGART, GERMANYbGEORG THIEME VERLAG KGcJUL  a2130-21360 v483 a<p>Starting from dimethyl (+/-)-2-hydroxy-3-methylenesuccinnate chemoenzymatic collective formal/total synthesis of enantiomerically pure bioactive natural products has been described via the advanced level common precursor (+)-artabotriol. An efficient enzymatic resolution with high enantiomeric purity, selective diester to diol reduction, and requisite dehydrative coupling reactions without any racemization are the significant topographies.</p>10a(+)-artabotriol10acollective synthesis10acoupling reactions10adimethyl (+/-)-2-hydroxy-3-methylenesuccinate10aEnzymatic resolution10aNatural products10areduction1 aBatwal, Ramesh, U.1 aArgade, N., P.  uhttps://library.ncl.res.in/content/chemoenzymatic-access-artabotriol-and-its-application-collective-synthesis-grandiamide-d