A series of pentyl-sulphonyl amidines was obtained using a multicomponent synthesis process. The rearrangement of unstable tosylazide-cyclopentanonenamine cycloadducts yielded a diazoalkane intermediate. This primary, unstable reaction product showed good reactivity with certain acid compounds in order to form the corresponding derivatives.
Multicomponent Synthesis of Pentyl-Sulfonyl Amidines via Diazoalkane / A. Contini, E. Erba, S. Pellegrino. - In: SYNLETT. - ISSN 0936-5214. - 2012:10(2012 Jun), pp. ST-2012-D0175-L.1523-ST-2012-D0175-L.1526.
Multicomponent Synthesis of Pentyl-Sulfonyl Amidines via Diazoalkane
A. ContiniPrimo
;E. ErbaSecondo
;S. PellegrinoUltimo
2012
Abstract
A series of pentyl-sulphonyl amidines was obtained using a multicomponent synthesis process. The rearrangement of unstable tosylazide-cyclopentanonenamine cycloadducts yielded a diazoalkane intermediate. This primary, unstable reaction product showed good reactivity with certain acid compounds in order to form the corresponding derivatives.
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