Results 61 to 70 of about 1,703,017 (234)
CXLI.—The rate of decomposition of diazo-compounds. Part I. Diazo-compounds of the benzene series [PDF]
J. Chem. Soc., Trans., 1902 n ...
Cain, John Cannell, Nicoll, Frank
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, 2016 A novel three-component coupling (3-CC) reaction of 2-aminoazines, aromatic aldehydes, and diazo-compounds producing polyfunctional β-amino-α-diazo-compounds has been developed.
Victoria Helan (1991983) +3 more
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XXII.—The rate of decomposition of diazo compounds. Part II. Diazo-compounds of the naphthalene series [PDF]
J. Chem. Soc., Trans., 1903 n ...
Cain, John Cannell, Nicoll, Frank
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Diazo Transfer Reactions to 1,3-Dicarbonyl Compounds with Tosyl azide
, 2011 International audienceA practical protocol for the large-scale preparation of 2-diazo-1,3-dicarbonyl compounds is described by diazo-transfer reactions with tosyl azide followed by efficient chromatographic purifications on silica gel and/or ...
Marc Presset +7 more
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Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2H)-one scaffold
Beilstein Journal of Organic Chemistry, 2022 A practically convenient and streamlined protocol for the trans-diastereoselective introduction of an aryl substituent at position 4 of the 1,4-dihydroisoquinol-3-one (1,4-DHIQ) scaffold is presented.
Dmitry Dar’in +3 more
doaj +1 more source
Recent Advances in the Synthesis of Aromatic Azo Compounds
Molecules, 2023 Aromatic azo compounds have -N=N- double bonds as well as a larger π electron conjugation system, which endows aromatic azo compounds with wide applications in the fields of functional materials.
Meng-Yun Zhao +2 more
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, 2014 Diazo compounds have great synthetic potential as versatile reagents in organic synthesis. The formation of Rh(II) carbenoids from diazo compounds allows the selective formation of C-C and C-heteroatom bonds and the introduction of functionality into ...
Schnaars, Christian
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Access to cyclopropanes with geminal trifluoromethyl and difluoromethylphosphonate groups
Beilstein Journal of Organic Chemistry, 2023 A synthetic route to the bench-stable fluorinated masked carbene reagent diethyl 2-diazo-1,1,3,3,3-pentafluoropropylphosphonate, bearing a trifluoromethyl and a difluoromethyl group is reported for the first time.
Ita Hajdin +5 more
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Angewandte Chemie International Edition, EarlyView.We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer +6 more
wiley +1 more source