@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}
}
@article {44495,
	title = {Synthetic studies towards Pseudoxylallemycin B, an antibiotic active against gram-negative bacteria: total synthesis of 3-epi-Pseudoxylallemycin B},
	journal = {Tetrahedron Letters},
	year = {2018},
	type = {Journal Article},
	abstract = {In an attempt towards the total synthesis of Pseudoxylallemycin B, a homo dimeric, N-methylated macrocyclic tetrapeptidic natural product, synthesis of its epimer at position 3 (d-Tyr instead of l-Tyr) is described here. During the course of synthesis we came across a striking yet unusual observation of complete epimerization which led to the formation of 3-epi-Pseudoxylallemycin B.},
	keywords = {Cyclic tetrapeptides, Epimerization, Gram-negative bacteria, Macrolactamization, Propyl phosphonic anhydride (T3P)},
	doi = {10.1016/j.tetlet.2018.06.028},
	author = {Gunjal, Vidya B.},
	editor = {Reddy, Shrinivasa D.}
}
