@article {42902,
	title = {Enantiospecific formal synthesis of inthomycin C},
	journal = {Chemistry Select},
	volume = {1},
	year = {2016},
	month = {MAR},
	pages = {495{\textendash}497},
	abstract = {<p>An enantiospecific synthesis of Hatakeyama{\textquoteright}s intermediate enynol has been accomplished in both enantiomeric forms. As these intermediates can be converted to (3R)-inthomycin C and (3S)-inthomycin C through respective enynol intermediates using reported procedures, present effort may be regarded as formal synthesis of inthomycin C in both enantiomeric forms. Our synthesis highlights the use of pantolactone chiral pool and thus reconfirms the previously assigned absolute stereochemistry as 3R to the natural product inthomycin C.</p>},
	doi = {10.1002/slct.201600128},
	author = {Athawale, Paresh R. and Kashinath, K. and Reddy, D. Srinivasa}
}
