@article {49680,
	title = {Total synthesis of ({\textpm})-streptoglyceride A and of putative ({\textpm})-streptoglyceride C},
	journal = {Organic Letters},
	volume = {27},
	year = {2025},
	month = {JUN},
	pages = {5931-5935},
	type = {Article},
	abstract = {<p>
	The first total synthesis of (+/-)-Streptoglyceride A-one of the early members of this family to be isolated-has been accomplished, along with the synthesis of the putative structure of (+/-)-Streptoglyceride C. The unique tricyclic ring present in these natural products has been constructed by employing a gold-catalyzed tandem diynol cycloisomerization followed by one-pot dihydroxylation/trans-glycosylation. The pendant diene unit was fabricated by Takai olefination and subsequent Stille coupling.</p>
},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.5c00879},
	author = {Khobragade, Virendra R. and Ramana, Chepuri V.}
}
