@article { ISI:000382768400020,
	title = {Total synthesis of (-)-nardoaristolone B},
	journal = {European Journal of Organic Chemistry},
	number = {22},
	year = {2016},
	month = {AUG},
	pages = {3804-3808},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {POSTFACH 101161, 69451 WEINHEIM, GERMANY},
	abstract = {<p>A stereoselective total synthesis of (-)-Nardoaristolone B, a nor-aristolane sesquiterpenoid natural product with an unusual 3/5/6 tricyclic ring system is described. The highlights of the present work includes use of (+)-(R)-Pulegone as a chiral-pool starting material, ring-closing metathesis, allylic oxidation and stereoselective cyclopropanation. In addition, a new analogue of Nardoaristolone B (minor product from the final step) was isolated in pure form and fully characterized with the help of single-crystal X-ray analysis.</p>},
	keywords = {Chiral pool, cyclopropanation, Nardoaristolone B, Natural products, Total synthesis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201600538},
	author = {Ople, Rohini S. and Handore, Kishor L. and Kamat, Nidhi S. and Reddy, D. Srinivasa}
}
