1236299-33-4

Upstream product

• 878289-48-6 1,4-dihydro-4-(phenylmethyl)-3H-furo[3,4-b]indol-3-one 
• 870-63-3 prenyl bromide 

Downstream Products

• 1236299-34-5 dimethyl 9-phenylmethyl-1-hydroxy-4-(3-methylbut-2-enyl)-9H-carbazole-2,3-dicarboxylate 

Relevant academic research and scientific papers

Lateral lithiation-initiated annulations in the synthesis of 1-oxygenated carbazole alkaloids and a cycloheptacarbazole

Anionic [4+2] annulation of lithiated furoindolones with dimethyl maleate followed by selective demethoxycarbonylation provides an efficient synthetic route to 3-methoxycarbonylcarbazoles. The route has led to the straightforward synthesis of two natural

A rapid entry to C-prenylcarbazoles: Total synthesis of clausamine C-D, clausevatine D and clausine F

The key prenylcarbazole precursor 33 was readily assembled from diester 30 by an ester-driven para-Claisen rearrangement followed by selective removal of the ester function. Unusual oxidative cyclization of 33 by m-CPBA resulted in the total synthesis of