@article { ISI:000335152300007,
	title = {Croncise organocatalytic route to protected (2S, 4R)-4-hydroxyornithine and(+)-pseudohygroline},
	journal = {Synlett},
	volume = {25},
	number = {8},
	year = {2014},
	month = {MAY},
	pages = {1089-1092},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A practical, efficient, and organocatalytic approach to the synthesis of (2S,4R)-4-hydroxyornithine and (+)-pseudohygroline is reported using proline-catalyzed sequential alpha-aminoxylation/alpha-amination reaction and Horner-Wadsworth-Emmons olefination reaction of an aldehyde as the key step.</p>},
	keywords = {aldehydes, Amination, Amino alcohols, cyclization, Enantioselectivity, Wittig reaction},
	issn = {0936-5214},
	doi = {10.1055/s-0033-1340977},
	author = {Jha, Vishwajeet 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}
}
