Regio- and Stereoselective Synthesis of Sulfur-Bearing Four-Membered Heterocycles: Direct Access to 2,4-Disubstituted Thietane 1-Oxides
Articolo
Data di Pubblicazione:
2015
Citazione:
Regio- and Stereoselective Synthesis of Sulfur-Bearing Four-Membered Heterocycles: Direct Access to 2,4-Disubstituted Thietane 1-Oxides / Degennaro, Leonardo; Carroccia, Laura; Parisi, Giovanna; Zenzola, Marina; Romanazzi, Giuseppe; Fanelli, Flavio; Pisano, Luisa; Luisi, Renzo. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - 80:24(2015), pp. 12201-12211. [10.1021/acs.joc.5b02126]
Abstract:
Starting from readily available C2-substituted thietane 1-oxides, a straightforward synthesis of new C2,C4-disubstituted thietane 1-oxides has been developed by using a lithiation/electrophilic trapping sequence. The chemical and configurational stability of lithiated C2-substituted thietane 1-oxides has been investigated as well as the stereochemical implications for this process. The results demonstrate that a stereoselective functionalization at the C2, C4 positions of a thietane is feasible, leaving intact the four-membered ring.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
NITROGEN STEREODYNAMICS; COMPLEXATION PHENOMENA; DRUG DISCOVERY; CHEMICAL SPACE; ALPHA; RING; FUNCTIONALIZATION; CARBANIONS; OXETANES; STRATEGIES
Elenco autori:
Degennaro, Leonardo; Carroccia, Laura; Parisi, Giovanna; Zenzola, Marina; Romanazzi, Giuseppe; Fanelli, Flavio; Pisano, Luisa; Luisi, Renzo
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