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Synthesis of Bi‑, Ter‑, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement

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NIAID Data Ecosystem2026-03-11 收录
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https://figshare.com/articles/dataset/Synthesis_of_Bi_Ter_and_Quaterpyridinecarboxylates_via_Propargylisoxazole_Pyridine_Rearrangement/12129579
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A flexible method was developed for the synthesis of 2,2′-bi-, 2,2′:6′,2″-ter-, and 2,2′:6′,2′′:6′′,2‴-quaterpyridines containing a nicotinic acid moiety. The approach involves the Fe­(II)/Au­(I)-catalyzed rearrangement of key 4-propargylisoxazole building blocks bearing a pyrid-2-yl or quinolin-2-yl substituent at the 3-position and Pd(0)-catalyzed cross-coupling reactions.
创建时间:
2020-04-08
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