Simple Synthesis of 3-Alkyl-1H-Indazoles Having Functional Groups At the ω-Position

Kazuyuki Sasakura Shionogi Research Laboratories, Shionogi & Co., Ltd., Fukushima-ku, Osaka, 553, Japan

Akiko Kawasaki Shionogi Research Laboratories, Shionogi & Co., Ltd., Fukushima-ku, Osaka, 553, Japan

Tsutomu Sugasawa Shionogi Research Laboratories, Shionogi & Co., Ltd., Fukushima-ku, Osaka, 553, Japan

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Süleyman Servi & Z. Rüstem Akgün. (2002) A NOVEL AND EFFICIENT SYNTHESIS OF 3-ARYL AND 3-HETEROARYL SUBSTITUTED-1H-INDAZOLES AND THEIR MANNICH DERIVATIVES. Synthetic Communications 32:22, pages 3399-3405.
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Deyi Zhang, Dan Kohlman, Joseph Krushinski, Sidney Liang, Bai-Ping Ying, John E. Reilly, Sean R. Dinn, David B. Wainscott, Suzanne Nutter, Wendy Gough, David L.G. Nelson, John M. Schaus & Yao-Chang Xu. (2004) Design, synthesis and evaluation of bicyclic benzamides as novel 5-HT1F receptor agonists. Bioorganic & Medicinal Chemistry Letters 14:24, pages 6011-6016.
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K. SASAKURA, A. KAWASAKI & T. SUGASAWA. (1988) ChemInform Abstract: Simple Synthesis of 3-Alkyl-1H-indazoles Having Functional Groups at the ?-Position.. ChemInform 19:36.
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Simple Synthesis of 3-Alkyl-1H-Indazoles Having Functional Groups At the ω-Position

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Simple Synthesis of 3-Alkyl-1H-Indazoles Having Functional Groups At the ω-Position

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