Controlled substance analgesic indole alkaloids

1.Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds:2.Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric

1.Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds:2.Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole.

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Application：3,6-Bis(methylthio)-1,2,4,5-tetrazine can be used as a versatile building block in the inverse elecron demand hetero Diels-Alder reactions. The Boger Research Group has reported this powerful approach in the synthesis of alkaloids.It can

Application：3,6-Bis(methylthio)-1,2,4,5-tetrazine can be used as a versatile building block in the inverse elecron demand hetero Diels-Alder reactions. The Boger Research Group has reported this powerful approach in the synthesis of alkaloids.It can

3-(1 5-DIAZABICYCLO(3.2.

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indole.

The Bio Basic 3-Indoleacetic Acid (IAA) with a composition of =100% 3-Indole acetic Acid (IAA), is suitable for use in laboratory research use only. It can be stored at a temperature of 18 to 25 degree C. Application: For Laboratory Research Use Only

The Bio Basic 3-Indoleacetic Acid (IAA) with a composition of =100% 3-Indole acetic Acid (IAA), is suitable for use in laboratory research use only. It can be stored at a temperature of 18 to 25 degree C. Application: For Laboratory Research Use Only