@article { ISI:000281783500005,
	title = {Short and efficient synthesis of (S)-(+)-2-(Hydroxymethyl)-6-piperidin-2-one},
	journal = {Synthesis-Stuttgart},
	number = {15},
	year = {2010},
	month = {AUG},
	pages = {2512-2514},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A concise synthesis of (S)-(+)-2-(hydroxymethyl)-6-piperidin-2-one is described that employs L-aspartic acid as chiral pool starting material and Wittig reaction as the key step.</p>},
	keywords = {Amino acid, Hydrogenation, L-aspartic acid, pipecolate, piperidone, Wittig reaction},
	issn = {0039-7881},
	doi = {10.1055/s-0029-1218823},
	author = {Upadhyay, Puspesh K. and Kumar, Pradeep}
}
@article {47427,
	title = {Short enantioselective total synthesis of (+)-tofacitinib},
	journal = {Tetrahedron Letters},
	volume = {67},
	year = {2021},
	month = {MAR},
	pages = {152838},
	type = {Article},
	abstract = {<p>An enantioselective total synthesis of Tofacitinib (CP-690,550), a Janus tyrosine kinase (JAK3) specific inhibitor has been achieved from the readily available 4-piperidone. Proline catalysed hydroxylation is the key step for the synthesis of enantiopure 1-benzyl-4-methylpiperidin-3-ol. (C) 2021 Elsevier Ltd. All rights reserved.</p>},
	keywords = {aminohydroxylation, Hydrogenation, L-proline, piperidone},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2021.152838},
	author = {Mane, Kishor D. and Kamble, Rohit B. and Suryavanshi, Gurunath}
}
