@article { ISI:000350219700005,
	title = {Synthesis of yangjinhualine A},
	journal = {Synthesis-Stuttgart},
	volume = {47},
	number = {4},
	year = {2015},
	month = {FEB},
	pages = {485-488},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Selective reduction of 3-(4-hydroxyphenyl)-2-methylmaleic anhydride provides access the corresponding gamma-hydroxybutenolide natural product yangjinhualine A.</p>},
	keywords = {anhydrides, lactones, Natural products, reduction, Regioselectivity},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1379582},
	author = {Deore, Prashant S. and Batwal, Ramesh U. and N. P. Argade}
}
@article { ISI:000380250800021,
	title = {Chemoenzymatic access to (+)-artabotriol and its application in collective synthesis of (+)-grandiamide D, (-)-tulipalin B, (+)-spirathundiol, and (+)-artabotriolcaffeate},
	journal = {Synthesis-Stuttgart},
	volume = {48},
	number = {13},
	year = {2016},
	month = {JUL},
	pages = {2130-2136},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<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>},
	keywords = {(+)-artabotriol, collective synthesis, coupling reactions, dimethyl (+/-)-2-hydroxy-3-methylenesuccinate, Enzymatic resolution, Natural products, reduction},
	issn = {0039-7881},
	doi = {10.1055/s-0035-1561588},
	author = {Batwal, Ramesh U. and N. P. Argade}
}
