The protonated lactam salts , 1, , 2, and , 3, were isolated from the non selective reaction of MoCl5 with δ-valerolactam in dichloromethane, carried out with different molar ratios. The 1:2 reaction of MoCl5 with N-methyl-2-pyrrolidone afforded the chloroiminium salt, 4, in 74% yield, together with minor amount of , 5. The products 1–5 were characterized by analytical and spectroscopic techniques, and by X-ray diffractometry in the cases of 1 and 3.

Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts / Fabio Marchetti;Guido Pampaloni;Stefano Zacchini. - In: RSC ADVANCES. - ISSN 2046-2069. - STAMPA. - 3:(2013), pp. 10007-10013. [10.1039/c3ra23305g]

Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts

ZACCHINI, STEFANO
2013

Abstract

The protonated lactam salts , 1, , 2, and , 3, were isolated from the non selective reaction of MoCl5 with δ-valerolactam in dichloromethane, carried out with different molar ratios. The 1:2 reaction of MoCl5 with N-methyl-2-pyrrolidone afforded the chloroiminium salt, 4, in 74% yield, together with minor amount of , 5. The products 1–5 were characterized by analytical and spectroscopic techniques, and by X-ray diffractometry in the cases of 1 and 3.
2013
Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts / Fabio Marchetti;Guido Pampaloni;Stefano Zacchini. - In: RSC ADVANCES. - ISSN 2046-2069. - STAMPA. - 3:(2013), pp. 10007-10013. [10.1039/c3ra23305g]
Fabio Marchetti;Guido Pampaloni;Stefano Zacchini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/191134
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