@article { ISI:000346037500028,
	title = {Total synthesis of deoxy-solomonamide B by mimicking biogenesis},
	journal = {Organic Letters},
	volume = {16},
	number = {23},
	year = {2014},
	month = {DEC},
	pages = {6148-6151},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A total synthesis of Deoxy-solomonamide B was accomplished starting from tryptophan in an efficient manner by mimicking the proposed biogenetic route. The present synthesis utilizes a crotylation, oxidative cleavage of the indole moiety, and macrolactamization as key steps. The use of the indole nucleus as a masked anthranilic acid unit paves the way for the easy synthesis of related macrocycles and natural products where the ortho-acyl aniline moiety is embedded into them, which otherwise is difficult to synthesize.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol503011g},
	author = {Vasudevan, N. and Kashinath, K. and Reddy, D. Srinivasa}
}
