@article {45351,
	title = {Total synthesis of (+)-trans- dihydronarciclasine from (+)-7-azabicyclo[2.2.1]heptanone},
	journal = {Tetrahedron },
	volume = {74},
	year = {2018},
	month = {SEP},
	pages = {5752-5757},
	type = {Article},
	abstract = {<p>A concise asymmetric total synthesis of Amaryllidaceae alkaloid (+)-trans-dihydronarciclasine is accomplished starting from optically pure 7-azabicyclo[2.2.1]heptanone scaffold in 13 linear steps. Key features of the strategy include substrate-directed stereoselective installation of the trans B-C ring junction and regioselective Wacker-type internal olefin oxidation to provide a rapid access to all hydroxyl functionalities over the key cyclohexane ring in a stereocontrolled manner. (C) 2018 Elsevier Ltd. All rights reserved.</p>},
	doi = {10.1016/j.tet.2018.08.016},
	author = {Pandey, Ganesh and Fernandes, Rushil and Dey, Debasis and Majumder, Binoy}
}
