Novel aspects on the reaction of trialkyl-(1-methylindol-2-yl)borates
作者:Minoru Ishikura、Masanao Terashima
DOI:10.1039/c39890000135
日期:——
A new use of trialkyl-(1-methylindol-2-yl)borates for the synthesis of 2-substituted indoles involving the palladium catalysed cross-coupling with vinylic and aromatic halides, or a facile alkyl migration from boron to carbon without an additional electrophile is described.
A novel C–C bond formation reaction with 1-methoxymethylindolylborateElectronic supplementary information (ESI) available: selected spectral data for compounds 4a, 6a, 6e (a pair of diastereoisomers) and 6g. See http://www.rsc.org/suppdata/cc/b1/b109880b/
作者:Minoru Ishikura、Hiromi Kato、Nobuyuki Ohnuki
DOI:10.1039/b109880b
日期:2002.1.30
The reaction of 1-methoxymethylindolylborates 2 with electrophiles
in the presence of benzaldehyde enabled the novel construction of tri-substituted
indoles in a âone-potâ procedure.
A Novel Aspect on the 1,2-Alkyl Migration Reaction with Trialkyl 1-Substituted Indol-2-ylborates
作者:Minoru Ishikura、Isao Agata
DOI:10.3987/com-95-7227
日期:——
Intramolecular 1,2-alkyl migration reaction of trialkyl(1-methoxyindol-2-yl)borates and trialkyl(1-methoxymethylindol-2-yl)borates gave rise to 2-alkylindoles and 2-alkyl-1-methylindoles, respectively.
ACTIVATORS OF THE RETINOIC ACID INDUCIBLE GENE "RIG-I" PATHWAY AND METHODS OF USE THEREOF
申请人:Kineta Immuno-Oncology LLC
公开号:US20200071316A1
公开(公告)日:2020-03-05
The present invention is directed to compounds of Formula (I), which are activators of the RIG-I pathway.