874667-99-9Relevant academic research and scientific papers
A divergent synthesis of triyne natural products and glycosylated analogues using a carbenoid rearrangement
Luu, Thanh,Shi, Wei,Lowary, Todd L.,Tykwinski, Rik R.
, p. 3167 - 3178 (2007/10/03)
Using a carbenoid rearrangement to introduce the conjugated acetylenic framework, a series of triynols has been synthesized in five steps from 1,4-butynediol. Several of the triyne alcohols are known natural products and others are glycosylated analogues.
