@article { ISI:000255698500035,
	title = {Carbohydrate-based approach for the total synthesis of aculeatin D and 6-epi-aculeatin D},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {10},
	year = {2008},
	month = {MAY},
	pages = {3915-3918},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A concise approach for the total synthesis of aculeatin D and 6-epi-aculeatin D employing differentially protected anti,anti-1,3,5-triol alkyne prepared from alpha-D-glucoheptonic-gamma-lactone derivative is documented. Phenol protecting group manipulation for selective O-debenzylation during the hydrogenation of the diyne intermediate and one-pot phenolic oxidation with concomitant spiroketalization highlight the accomplished total synthesis.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo800026n},
	author = {Ramana, C. V. and Srinivas, Burgula}
}
