Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system

The Leimgruber-Batcho Indole Synthesis

Robin D. Clark, David B. Repke · Heterocycles · 1984 · 133 citations · Full text

Natural Sciences, Chemistry, Medicinal Chemistry +12

Microwave assisted Leimgruber–Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines

Jason Siu, Ian R. Baxendale, Steven V. Ley · Organic & Biomolecular Chemistry · 2004 · 98 citations · Full text

Natural Sciences, Chemical Engineering, Chemistry +16

The Serotonin 5-HT4 Receptor. 2. Structure-Activity Studies of the Indole Carbazimidamide Class of Agonists

Karl‐Heinz Buchheit, R. Gamse, Rudolf Giger et al. · Journal of Medicinal Chemistry · 1995 · 79 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +15

Synthesis of .alpha.-monosubstituted indoles

Robert L. Augustine, A. J. Gustavsen, S. F. WANAT et al. · The Journal of Organic Chemistry · 1973 · 59 citations

Natural Sciences, Chemistry, Medicinal Chemistry +8

CATALYTIC REDUCTION OF AROMATIC NITRO COMPOUNDS WITH HYDRAZINE IN THE PRESENCE OF IRON(III) CHLORIDE AND ACTIVE CARBON

Tsuneaki Hirashima, Osamu Manabe · Chemistry Letters · 1975 · 55 citations

Natural Sciences, Chemical Engineering, Chemistry +8