@article { ISI:000296873900005,
	title = {Asymmetric first total syntheses and assignment of absolute configuration of oxazinin-5, oxazinin-6 and preoxazinin-7},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {9},
	number = {23},
	year = {2011},
	month = {SEP},
	pages = {7990-7992},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Asymmetric first total syntheses of the unprecedented toxins oxazinin-5, oxazinin-6 and preoxazinin-7 have been achieved from a common key intermediate 18, derived from a regiocontrolled Sharpless asymmetric aminohydroxylation and oxa-Michael reaction, which in addition to confirming the structure also established the absolute configuration of the natural products. On the way an expeditious synthesis of a metabolite bursatellin was completed in 8 steps.</p>},
	issn = {1477-0520},
	doi = {10.1039/c1ob06320k},
	author = {Dethe, Dattatraya H. and Ranjan, Alok and Pardeshi, Vijendra H.}
}
@article { ISI:000289455200019,
	title = {Biomimetic total syntheses of flinderoles B and C},
	journal = {Journal of the American Chemical Society},
	volume = {133},
	number = {9},
	year = {2011},
	month = {MAR},
	pages = {2864-2867},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A simple and efficient biomimetic synthesis of pyrrolo[1,2-a]indoles using a highly stereo- and regioselective [3 + 2] reaction cascade was developed and then further applied in the first total synthesis of flinderoles B and C, which proceeded in 17.2\% yield over the longest linear sequence of 11 steps.</p>},
	issn = {0002-7863},
	doi = {10.1021/ja1116974},
	author = {Dethe, Dattatraya H. and Erande, Rohan D. and Ranjan, Alok}
}
