1379449-95-2Relevant academic research and scientific papers
A total synthesis prompts the structure revision of haouamine B
Matveenko, Maria,Liang, Guangxin,Lauterwasser, Erica M. W.,Zubia, Eva,Trauner, Dirk
supporting information; experimental part, p. 9291 - 9295 (2012/07/14)
A concise asymmetric approach to the indeno-tetrahydropyridine core of the unusual alkaloid haouamine B allowed for an investigation of a biomimetic oxidative phenol coupling as a proposed biosynthetic step, and ultimately provided access to the published structure of the natural product. As a consequence of our synthetic studies, the structure of haouamine B has been revised.
