196213-29-3Relevant academic research and scientific papers
The first stereospecific synthesis of michellamine B
Hobbs, Peter D.,Upender, Velaparthi,Liu, Jyanwei,Pollart, Daniel J.,Thomas, David W.,Dawson, Marcia I.
, p. 923 - 924 (1996)
The dimeric alkaloid michellamine B is synthesized stereospecifically by the palladium-catalysed cross-coupling of the 6'-naphthaleneboronic acid of the tetrabenzylated derivative of korupensamine A and the 6'-bromo analogue of the tetrabenzylated derivat
Stereospecific Syntheses of Michellamines A and C
Hobbs, Peter D.,Upender, Velaparthi,Dawson, Marcia I.
, p. 965 - 967 (1997)
The total syntheses of two of the three dimeric naphthylisoquinoline michellamines - A and C - were achieved by Pd-catalyzed cross-coupling of the appropriate 6′-bromo- or 6′-boronic acid-substituted tetrabenzylated korupensamine A and B derivatives under nonaqueous conditions, followed by deprotection of the octabenzylated products.
