@article { ISI:000285311000016,
	title = {Enantio- and diastereocontrolled total synthesis of (+)-strictifolione},
	journal = {European Journal of Organic Chemistry},
	number = {36},
	year = {2010},
	month = {DEC},
	pages = {6993-7004},
	publisher = {WILEY-BLACKWELL},
	address = {COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA},
	abstract = {<p>A concise and practical enantioselective synthesis of (+)-strictifolione has been achieved in high diastereomeric excess using Jacobsen{\textquoteright}s hydrolytic kinetic resolution, proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons olefination of aldehyde and cross olefin/ring-closing metathesis as the key steps.</p>},
	keywords = {Asymmetric synthesis, Hydrolytic kinetic resolution, lactones, Natural products, organocatalysis, Ring-closing metathesis, Total synthesis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201001221},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Naidu, S. Vasudeva and Dhavale, Dilip D.}
}
@article { ISI:000371239900016,
	title = {Enantioselective modular total synthesis of macrolides Sch725674 and C-4-epi-Sch725674},
	journal = {European Journal of Organic Chemistry},
	number = {6},
	year = {2016},
	month = {FEB},
	pages = {1215-1226},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {POSTFACH 101161, 69451 WEINHEIM, GERMANY},
	abstract = {<p>The convergent total synthesis of Sch725674 has been accomplished by starting from (R)-1,2-epoxyheptane and assembling five modules in a highly stereoselective manner to give the final product in 6.6\% overall yield. The same strategy was extended to the synthesis of its C-4 epimer. Key reactions of the synthetic pathway include a Jacobsen hydrolytic kinetic resolution of an epoxide followed by its regioselective opening through a Yamaguchi-Hirao alkynylation, and ring-closing metathesis reaction to furnish the unique 14-membered ring macrolactone. In addition, the influence of protecting groups on the efficiency of the ring-closing metathesis (RCM) macrocyclization has been studied to maximize its yields.</p>},
	keywords = {Asymmetric synthesis, Hydrolytic kinetic resolution, Macrocycles, Metathesis, Natural products},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201501531},
	author = {Sharma, Brijesh M. and Gontala, Arjun and Kumar, Pradeep}
}
