124337-87-7Relevant academic research and scientific papers
Synthetic studies on the ambiguine family of alkaloids: Construction of the ABCD ring system
Rafferty, Ryan J.,Williams, Robert M.
, p. 2037 - 2040 (2011)
A racemic synthesis of the ABCD ring core of the ambiguines that preserves the tertiary alcohol has been accomplished in a convergent synthesis in 10 synthetic steps, in an overall yield of 46% from commercially available 4-bromoindole and m-methylanisole
SYNTHETIC STUDIES OF MARINE ALKALOIDS HAPALINDOLES. Part 1. TOTAL SYNTHESIS OF (+/-)-HAPALINDOLES J and M
Muratake, Hideaki,Natsume, Mitsutaka
, p. 6331 - 6342 (2007/10/02)
The first concise synthesis of marine indole alkaloids (+/-) hapalindoles J (4) and M (5) was achieved in seven or six steps starting from a readily available compound 6 using important key reactions, 6 -> 7 -> 8 and 35 -> 41 or 5.
