@article { ISI:000347229500001,
	title = {One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {13},
	number = {4},
	year = {2015},
	month = {OCT},
	pages = {970-973},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Multiple reactions in one pot has always been a useful technique for synthetic organic chemists, as it can minimizes solvent usage, time and the number of purification steps when compared to individual multi-step syntheses. In line with this, here in this perspective we discuss a one-pot quadruple/triple reaction sequence comprising an enyne ring-closing metathesis/cross-metathesis/Diels-Alder/aromatization for the synthesis of natural products setting.</p>},
	issn = {1477-0520},
	doi = {10.1039/c4ob02143f},
	author = {Kashinath, K. and Reddy, D. Srinivasa}
}
@article {46888,
	title = {Overturning the peribysin family natural products isolated from periconia byssoides OUPS-N133: synthesis and stereochemical revision of peribysins A, B, C, F, and G},
	journal = {Organic Letters},
	volume = {22},
	year = {2020},
	month = {APR},
	pages = {3104-3109},
	type = {Article},
	abstract = {<p>Herein we report the stereochemical revision of peribysins A, B, C, F, and G, guided by enantiospecific total synthesis starting from (+)-nootkatone. Furthermore, we reconfirmed the absolute stereochemistry of peribysin Q The highlights of the synthesis are enone transposition and kinetic iodination resulting in separation of diastereomers. Our findings coupled with synthetic and biological data previously reported by Danishefsky{\textquoteright}s group suggest that the original stereochemistries of peribysins A, B, C, F, and G were misassigned.</p>
},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.0c00857},
	author = {Athawale, Paresh R. and Kalmode, Hanuman P. and Motiwala, Zenia and Kulkarni, Kiran A. and Reddy, D. Srinivasa}
}
@article {47680,
	title = {One-pot oxidation of secondary alcohols to alpha-hydroxy ketones: application to synthesis of oxoaplysinopsin D, E, F, \& G},
	journal = {European Journal of Organic Chemistry},
	volume = {2021},
	year = {2021},
	month = {APR },
	pages = {2188-2192},
	type = {Article},
	abstract = {A simple one-pot transformation of secondary alcohols to alpha-hydroxy ketones using pyridinium dichromate (PDC) in DMF has been developed and substrate scope tested with 25 compounds of hydantoin derivatives. Using this method, we have devised a common dihydroxy intermediate and synthesized four natural products oxoaplysinopsins D, E, F, and G for the first time.},
	keywords = {alpha-Hydroxylation, Hydantoin, Natural product, Oxoaplysinopsin, Retro-aldol},
	issn = {1434-193X},
	doi = {10.1002/ejoc.202100184},
	author = {Kulkarni, Akshay S. and Ramesh, Eagala and Reddy, D. Srinivasa}
}
