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Beilstein J. Org. Chem. 2024, 20, 1396–1404, doi:10.3762/bjoc.20.121
Graphical Abstract
Figure 1: Biologically active pyrazole–triazole hybrids 1–4: inhibitory effect on cholera bacteria [13], antimicr...
Scheme 1: Literature-reported synthetic routes to pyrazole–triazole hybrids: synthesis of azides 7 or 8 from ...
Scheme 2: Synthesis of pyrazolyl azides 19a–v via cleavage of the protecting triazene moiety. For compounds 1...
Scheme 3: Synthesis of pyrazole–triazole hybrids via CuAAC and ORTEP diagrams of triazole products 21sd and 2...
Figure 2: Synthesized triazole–pyrazole hybrids 21aa–vg.
Scheme 4: One-pot synthesis of triazole–pyrazole hybrid 21gd. aOne-pot setup yielded 21gd with unknown impuri...
Scheme 5: Solid-phase synthesis of azidopyrazole 19g and triazole–pyrazole hybrid 21gd by immobilization of a...
Beilstein J. Org. Chem. 2018, 14, 515–522, doi:10.3762/bjoc.14.37
Scheme 1: Previously reported procedure for the addition of ketene dithioacetals to α,β-unsaturated ketones [33] ...
Scheme 2: Addition of dithi(ol)anylium TFBs to α,β-unsaturated non-cyclic ketones.
Scheme 3: Addition of dithi(ol)anylium TFBs to α,β-unsaturated cyclic ketones.
Scheme 4: Single versus double addition of ketones to dithiolanylium TFB 1e. adr was calculated from the 1H N...
Scheme 5: The scope of the presented protocol demonstrated by examples including the use of additional electr...
Scheme 6: Synthesis of diene dithioacetals 18a and 18b by addition of ynone 17 to α-alkyl or aryl-substitued ...