4-Phenyl-3,4-dihydro-β-carboline was prepared using the Bischler-Napieralski reaction on β-phenyltryptamine. 2004 Springer Science + Business Media, Inc.
The base-free van Leusen reaction of cyclic imines on water: Synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives
Construction of imidazoles has been demonstrated on water under base-free conditions. The reaction of dihydro β-carboline imines and p-toluenesulfonylmethyl isocyanides furnished the corresponding substituted N-fused imidazo 6,11-dihydro β-carboline derivatives in very good yields under ambient conditions. The use of deuterium oxide (D2O) as a solvent enabled the incorporation of deuterium isotopes in the imidazole ring.
Satyam, Killari,Murugesh,Suresh, Surisetti
p. 5234 - 5238
(2019/06/07)
4-SUBSTITUTED BETA-CARBOLINES AS IMMUNOMODULATORS
This invention relates to 4-substituted beta -carbolines and beta -carboline analogs that inhibit Ca+2 influx and interleukin-2 (IL-2) production. The 4-substituted beta -carbolines and beta -carboline analogs of this invention are represented by formula
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(2008/06/13)
4-substituted beta-carbolines and analogs thereof
This invention relates to 4-substituted beta -carbolines and beta -carboline analogs that inhibit Ca+2 influx and interleukin-2 (IL-2) production. The 4-substituted beta -carbolines and beta -carboline analogs of this invention are represented by formula
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(2008/06/13)
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