@article { ISI:000326290300011,
	title = {Synthesis of C-disaccharides through a one-pot alkynol cycloisomerization-reductive deoxygenation},
	journal = {Chemistry-A European Journal},
	volume = {19},
	number = {45},
	year = {2013},
	month = {NOV},
	pages = {15109-15114},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	keywords = {C-disaccharides, carbohydrates, Epoxide-alkyne coupling, Gold catalysis, Reductive deoxygenation},
	issn = {0947-6539},
	doi = {10.1002/chem.201302252},
	author = {Narute, Sachin B. and Rout, Jeetendra Kumar and Ramana, Chepuri V.}
}
@article {49652,
	title = {Attempted synthesis of the central 2,2-disubstituted pseudoindoxyl core of Austamide via a [Au]-catalyzed nitroalkyne cycloisomerization and intramolecular [3+2]-cycloaddition},
	journal = {Tetrahedron},
	volume = {167},
	year = {2024},
	month = {NOV },
	pages = {134301},
	type = {Article},
	abstract = {<p>
	Herein, we describe an Au-catalyzed cycloisomerization process of a nitroalkyne that was projected to construct the central 2,2-disubstituted pseudoindoxyl core of the natural product Austamide. Our intended strategy for forging the pseudoindoxyl core is based on the nitroalkyne cycloisomerization followed by a subsequent intramolecular [3 + 2] cycloaddition. However, the [3 + 2] cycloaddition occurred in an undesired manner, ultimately leading to a complex hexacyclic scaffold.</p>
},
	keywords = {Austamide, Gold catalysis, Intramolecular [3+2] cycloaddition, Nitroalkyne cycloisomerization},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2024.134301},
	author = {Halnor, Swapnil V. and Ramana, Chepuri V.}
}
