A cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction has been conveniently used in an expeditious synthetic approach to light-driven Z/E molecular switches featuring an imine function conjugated to olefin groups that mimics natural protonated Schiff bases. © 2007 Elsevier Ltd. All rights reserved.
Zanirato, V., Pollini, G.P., DE RISI, C., Valente, F., Melloni, A., Fusi, S., et al. (2007). Synthesis of bio-mimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction. TETRAHEDRON, 63(23), 4975-4982 [10.1016/j.tet.2007.03.141].
Synthesis of bio-mimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction
FUSI S.;OLIVUCCI M.
2007-01-01
Abstract
A cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction has been conveniently used in an expeditious synthetic approach to light-driven Z/E molecular switches featuring an imine function conjugated to olefin groups that mimics natural protonated Schiff bases. © 2007 Elsevier Ltd. All rights reserved.
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https://hdl.handle.net/11365/19456
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