In this chapter, alkene synthesis based on the reaction of N-tosylhydrazones is described. The reactivity of tosylhydrazones is determined by either the acidity of alpha-proton and hydrazone proton or the electropositivity of the carbon of C-N bond. This leads to diverse reactivities and a series of N-tosylhydrazone-based olefination methodologies. Both non-catalytic and transition metal-catalyzed olefinations from N-tosylhydrazones are introduced in this chapter. Most of the transition metal-catalyzed reactions proceed via metal carbene transformations. The synthesis of alkenes through Pd-catalyzed cross-coupling reactions of N-tosylhydrazones is particularly attractive and will be discussed in detail.
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Univ Nova Lisboa, Fac Ciencias & Tecnol, P-2829516 Caparica, PortugalUniv Nova Lisboa, Fac Ciencias & Tecnol, P-2829516 Caparica, Portugal
Pires, Marina J. Dias
Poeira, Diogo L.
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机构:Univ Nova Lisboa, Fac Ciencias & Tecnol, P-2829516 Caparica, Portugal
Poeira, Diogo L.
Marques, M. Manuel B.
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Univ Vienna, Inst Organ Chem, A-1010 Vienna, Austria
New Univ Lisbon Requimte, Fac Sci & Technol, Lisbon, PortugalUniv Nova Lisboa, Fac Ciencias & Tecnol, P-2829516 Caparica, Portugal
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Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Synthet Rubber, Changchun 130022, Jilin, Peoples R ChinaDalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
Xu, Peng
Han, Fu-She
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Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Synthet Rubber, Changchun 130022, Jilin, Peoples R ChinaDalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
Han, Fu-She
Wang, Yan-Hua
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Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R ChinaDalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China