@article { ISI:000354004400014,
	title = {Breaking and making of olefins simultaneously using ozonolysis: application to the synthesis of useful building blocks and macrocyclic core of solomonamides},
	journal = {Organic Letters},
	volume = {17},
	number = {9},
	year = {2015},
	month = {MAY},
	pages = {2090-2093},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A simple and practical one-pot) two-directional approach to access olefinic esters through simultaneous breaking and making of olefins using ozonolysis of alkenyl aryl selenides is disclosed The scope of the method with a variety of example{\textquoteright}s is demonstrated, and the end products obtained here are useful building blocks. As a direct application of the present method,the macrocyclic cote of potent anti-inflammatory natural cyclic peptides, solomonamides, is synthesized.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.5b00637},
	author = {Kashinath, K. and Dhara, Santu and Reddy, D. Srinivasa}
}
@article {42897,
	title = {Solution-phase synthesis of the macrocyclic core of teixobactin},
	journal = {European Journal of Organic Chemistry},
	volume = {25},
	year = {2016},
	month = {SEP},
	pages = {4289-4293},
	abstract = {<p>Towards the total chemical synthesis of the exceptionally potent antibiotic teixobactin, we synthesized the macrocyclic core of a natural product by using a solution-phase approach. The gramscale synthesis of L-allo-enduracididine and Shiina macrolactonization are highlights of the present disclosure.</p>},
	author = {Dhara, Santu and Gunjal, Vidya B. and Handore, Kishor L. and Reddy, D. Srinivasa}
}
