@article { ISI:000358099300015,
	title = {Enantioselective synthesis of (+)-hygroline and (+)-pseudohygroline via Keck allylation and CBS reduction},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {32},
	year = {2015},
	month = {AUG},
	pages = {4704-4705},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An enantioselective synthesis of (+)-hygroline and (+)-pseudohygroline has been achieved in high optical purity (98\% ee) from readily available 1,4-butanediol. The synthesis strategy employs a Keck allylation, CBS reduction, and Wacker oxidation. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {CBS reduction, Keck allylation, Pyrrolidines, Wacker oxidation},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.06.012},
	author = {Bhoite, Shubhangi P. and Kamble, Rohit B. and Suryavanshi, Gurunath M.}
}
@article {49124,
	title = {Enantioselective synthesis of (+)-Sedridine, (-)-Allosedridine and their N-Methyl analogs via Maruoka-Keck allylation and CBS reduction},
	journal = {Natural Product Research },
	volume = {37},
	year = {2023},
	month = {OCT},
	pages = {3388-3394},
	type = {Article},
	abstract = {<p>
	A simple synthetic approach has been developed for the enantioselective total synthesis of (+)-Sedridine, (-)-Allosedridine and their analogs such as (+)-N- Methyl Sedridine and (-)-N-Methylallosedridine. The synthesis was achieved by using commercially available starting materials via Maruoka-Keck allylation, Wacker oxidation, and CBS reduction. The synthetic root provides a good diastereomeric ratio and high yields.</p>
},
	keywords = {CBS reduction, Maruoka-Keck allylation, Piperidine, Wacker oxidation},
	issn = {1478-6419},
	doi = {10.1080/14786419.2022.2076229},
	author = {Bhoite, Shubhangi P. and Suryavanshi, Gurunath}
}
