@article { ISI:000379455300035,
	title = {Total synthesis of the marine natural product solomonamide B necessitates stereochemical revision},
	journal = {Organic Letters},
	volume = {18},
	number = {13},
	year = {2016},
	month = {JUL},
	pages = {3178-3181},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of the proposed structure of solomonamide B has been achieved. However, the H-1 and C-13 NMR spectral data of the synthesized compound was not exactly matching with that of the natural solomonamide B. This prompted us to revise the originally proposed structure, in particular, the stereochemistry of the nonpeptide part, which was confirmed by its total synthesis. During the course of the synthesis, we have developed an interesting hydroxy group directed Wacker oxidation of internal olefins in a macrocyclic setting.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.6b01395},
	author = {Kashinath, K. and Jachak, Gorakhnath R. and Athawale, Paresh R. and Marelli, Udaya Kiran and Gonnade, Rajesh G. and Reddy, D. Srinivasa}
}
