50624-08-3Relevant academic research and scientific papers
Skeletal diversity construction via a branching synthetic strategy
Wyatt, Emma E.,Fergus, Suzanne,Galloway, Warren R. J. D.,Bender, Andreas,Fox, David J.,Plowright, Alleyn T.,Jessiman, Alan S.,Welch, Martin,Spring, David R.
, p. 3296 - 3298 (2008/09/19)
A branching synthetic strategy was used to efficiently generate structurally diverse scaffolds, which span a broad area of chemical descriptor space, and their biological activity against MRSA was demonstrated. The Royal Society of Chemistry 2006.
Synthesis of furocoumarins: Part 33 - Synthesis of 6/7-methoxy-8/9-methylcycloalkenopsoralens
Soman, Shubhangi S,Trivedi, K N
, p. 30 - 34 (2007/10/02)
Synthesis of psoralen derivatives such as 7-methoxy-9-methyl-5-(H)-oxobenzofurobenzopyran (10), its tetrahydro derivative (13) and 6-methoxy-8-methyl-4-oxo-1,2,3,4-tetrahydrocyclopentafurobenzopyran (23) has been carried out by Claisen rearrangement of the corresponding allyl ethers followed by cyclisation and dehydrogenation.To obtain 23, dehydrogenation has been carried out by employing palladium (II)bis(benzonitrile) dichloride.
