A stereocontrolled synthesis of (2S,3R)-3-hydroxyproline 1, and trans-(2R,3S)-2-hydroxymethyl-3-hydroxypyrrolidine 2 has been achieved in 21% and 38% yield via the homochiral 4,5-disubstituted oxazolidin-2-one 3. The trans relationship in 2 has been introduced by a modified Mitsunobu reaction.

A straightforward synthesis of (2S,3R)-3-hydroxyproline and trans-(2R,3S)-2-hydroxymethyl-3-hydroxypyrrolidine / Natalina, Dell'Uomo; Maria Cristina Di, Giovanni; Misiti, Domenico; Giovanni, Zappia; Giuliano Delle, Monache. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - STAMPA. - 7:1(1996), pp. 181-188. [10.1016/0957-4166(95)00434-3]

A straightforward synthesis of (2S,3R)-3-hydroxyproline and trans-(2R,3S)-2-hydroxymethyl-3-hydroxypyrrolidine

MISITI, Domenico;
1996

Abstract

A stereocontrolled synthesis of (2S,3R)-3-hydroxyproline 1, and trans-(2R,3S)-2-hydroxymethyl-3-hydroxypyrrolidine 2 has been achieved in 21% and 38% yield via the homochiral 4,5-disubstituted oxazolidin-2-one 3. The trans relationship in 2 has been introduced by a modified Mitsunobu reaction.
1996
01 Pubblicazione su rivista::01a Articolo in rivista
A straightforward synthesis of (2S,3R)-3-hydroxyproline and trans-(2R,3S)-2-hydroxymethyl-3-hydroxypyrrolidine / Natalina, Dell'Uomo; Maria Cristina Di, Giovanni; Misiti, Domenico; Giovanni, Zappia; Giuliano Delle, Monache. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - STAMPA. - 7:1(1996), pp. 181-188. [10.1016/0957-4166(95)00434-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/8288
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