New tetrahydro-3aH-cyclopenta[d][1,3]thiazolines and hexahydro-1,3-benzothiazolines were obtained in satisfactory yields by reaction of cycloalkenyl-1-diazenes with thioamides These thiazolines were converted into unknown fused cycloalkyl-thiazoline-pyrazole systems. (c) 2007 Elsevier Ltd. All rights reserved.

Attanasi, O.A., Berretta, S., De Crescentini, L., Favi, G., Filippone, P., Giorgi, G., et al. (2007). Unexpected regioselectivity in the reaction between cycloalkenyl-1-diazenes and thioamides: useful entry to fused cycloalkyl-thiazoline and cycloalkyl-thiazoline-pyrazole systems. TETRAHEDRON LETTERS, 48(14), 2449-2451 [10.1016/j.tetlet.2007.02.041].

Unexpected regioselectivity in the reaction between cycloalkenyl-1-diazenes and thioamides: useful entry to fused cycloalkyl-thiazoline and cycloalkyl-thiazoline-pyrazole systems

Giorgi, G.;
2007-01-01

Abstract

New tetrahydro-3aH-cyclopenta[d][1,3]thiazolines and hexahydro-1,3-benzothiazolines were obtained in satisfactory yields by reaction of cycloalkenyl-1-diazenes with thioamides These thiazolines were converted into unknown fused cycloalkyl-thiazoline-pyrazole systems. (c) 2007 Elsevier Ltd. All rights reserved.
2007
Attanasi, O.A., Berretta, S., De Crescentini, L., Favi, G., Filippone, P., Giorgi, G., et al. (2007). Unexpected regioselectivity in the reaction between cycloalkenyl-1-diazenes and thioamides: useful entry to fused cycloalkyl-thiazoline and cycloalkyl-thiazoline-pyrazole systems. TETRAHEDRON LETTERS, 48(14), 2449-2451 [10.1016/j.tetlet.2007.02.041].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/10142
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