@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}
}
@article {44462,
	title = {Efforts to access the potent antitrypanosomal marine natural product janadolide: synthesis of des- tert -butyl janadolide and its biological evaluation},
	journal = {ACS Omega},
	year = {2018},
	month = {FEB},
	abstract = {To identify novel antitrypanosomal agents based on Janadolide, a potent macrocyclic polyketide{\textendash}peptide hybrid, a macrolactonization strategy was explored. We prepared des-tert-butyl Janadolide and evaluated its antitrypanosomal activity. Our findings suggest that the tert-butyl group is necessary for the desired bioactivity.},
	doi = {10.1021/acsomega.7b01920},
	author = {Athawale, Paresh R. and Jachak, Gorakh and Shukla, Anurag and Shanmugam, Dhanasekaran and Reddy, Srinivasa}
}
