Trushkov IV, Uchuskin MG, Abaev VT, Serdyuk O (2019)
Publication Type: Journal article, Review article
Publication year: 2019
Book Volume: 51
Pages Range: 787-815
Journal Issue: 4
Indolylvinyl ketones are valuable building blocks that can be utilized for the synthesis of numerous natural products and bioactive molecules containing an indole core motif. Herein, we describe their application for the total synthesis of some alkaloids, their analogues, and a variety of other important compounds, with an emphasis on biologically active examples. 1Introduction 2 Functionalization of the Enone C=C Bond 2.1 Reduction 2.2 Michael Addition 2.3 Cycloaddition 3 Transformation of the Carbonyl Group 3.1 Reduction 3.2 Knoevenagel Reaction 3.3 Addition of Organometallic Compounds 3.4 Olefination 4 Reactions Involving the Enone Conjugate System C=C-C=? 4.1 Reactions with 1,2-Dinucleophiles 4.2 Reactions with Compounds Bearing an Active Methylene Group 4.3 Reactions with 1,3-Dinucleophiles 4.4 Reactions with 1,4-Dinucleophiles
APA:
Trushkov, I.V., Uchuskin, M.G., Abaev, V.T., & Serdyuk, O. (2019). Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds. Synthesis-Stuttgart, 51(4), 787-815. https://dx.doi.org/10.1055/s-0037-1611702
MLA:
Trushkov, Igor V., et al. "Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds." Synthesis-Stuttgart 51.4 (2019): 787-815.
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