4.5 Article

One-Pot Regioselective Synthesis of 3-Benzylthiazolo[3,2-a]indoles by Sequential Sonogashira Coupling Followed by Triethylamine-Induced Cyclization

期刊

SYNTHESIS-STUTTGART
卷 -, 期 9, 页码 1413-1418

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0030-1259971

关键词

Sonogashira coupling; palladium catalyst; base-promoted cyclization; aryl iodide; thiazoloindole

资金

  1. CSIR (New Delhi)
  2. DST (New Delhi)

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A number of 2-(prop-2-ynylthio)-1H-indoles have been utilized for the synthesis of 3-benzylthiazolo[3,2-a]indoles by Sonogashira acetylide-coupling followed by triethylamine-induced regioselective cyclization in a one-pot operation. The cyclization is dependent on the nature of the substituents on the phenyl ring of the substrates.

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