@article { ISI:000282106400002,
	title = {Concise synthesis of (2S,3S,4S)-2-(Hydroxymethyl)pyrrolidine-3,4-diol (LAB1)},
	journal = {Synthesis-Stuttgart},
	number = {18},
	year = {2010},
	month = {SEP},
	pages = {3063-3066},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The synthesis of (2S,3S,4S)-2-(hydroxymethyl)pyrrolidine-3,4-diol (LAB1) from Garner{\textquoteright}s aldehyde is described using the Sharpless asymmetric dihydroxylation as the key step.</p>},
	keywords = {alkaloid, azasugars, diastereoselectivity, Garner{\textquoteright}s aldehyde, pyrrolidine, Wittig reaction},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1258185},
	author = {Upadhyay, Puspesh K. and Kumar, Pradeep}
}
@article {49306,
	title = {Organocatalytic route to the enantioselective synthesis of syn/ anti-α-hydrazino-γ-fluoro alcohols},
	journal = {Tetrahedron Letters},
	volume = {145},
	year = {2024},
	month = {JUL},
	pages = {155179},
	type = {Article},
	abstract = {<p>
	A general organocatalytic method has been developed for the asymmetric synthesis of alpha-hydrazino-gamma-fluoro alcohols, a precursor to syn/anti-1,3-fluoro amines. The strategy employs alpha-fluorination catalyzed by prolinederived catalyst, (S)-alpha,alpha-bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemetha nol trimethylsilyl ether followed by Horner-Wadsworth-Emmons (HWE) olefination of aldehydes, and proline-catalyzed alpha-amination as the key steps. The title compounds showed excellent diastereoselectivity (up to 99:1) and enantioselectivity (up to 99 \%).</p>
},
	keywords = {alpha-Amination, alpha-Fluorination, diastereoselectivity, Enantioselectivity, HWE olefination, organocatalyst},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2024.155179},
	author = {Khonde, Nilesh S. and Said, Madhukar S. and Danve, Shivam S. and Kumar, Pradeep}
}
