A strategy for the stereoselective functionalization of thietane 1-oxide has been developed. Mono (C2 substituted) and doubly (C2, C4 disubstituted) functionalized thietanes have been obtained from the readily available thietane 1-oxide by using the corresponding organometallic intermediates that reacted with electrophiles leaving intact the 4-membered ring.

Straightforward access to 4-membered sulfurated heterocycles: Introducing a strategy for the single and double functionalization of thietane 1-oxide / Carroccia, L.; Degennaro, L.; Romanazzi, Giuseppe; Cuocci, C.; Pisano, L.; Luisi, R.. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0520. - 12:14(2014), pp. 2180-2184. [10.1039/c4ob00173g]

Straightforward access to 4-membered sulfurated heterocycles: Introducing a strategy for the single and double functionalization of thietane 1-oxide

ROMANAZZI, Giuseppe;
2014-01-01

Abstract

A strategy for the stereoselective functionalization of thietane 1-oxide has been developed. Mono (C2 substituted) and doubly (C2, C4 disubstituted) functionalized thietanes have been obtained from the readily available thietane 1-oxide by using the corresponding organometallic intermediates that reacted with electrophiles leaving intact the 4-membered ring.
2014
Straightforward access to 4-membered sulfurated heterocycles: Introducing a strategy for the single and double functionalization of thietane 1-oxide / Carroccia, L.; Degennaro, L.; Romanazzi, Giuseppe; Cuocci, C.; Pisano, L.; Luisi, R.. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0520. - 12:14(2014), pp. 2180-2184. [10.1039/c4ob00173g]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11589/1163
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