80034-90-8Relevant articles and documents
Efficient and selective iron-mediated reductive Claisen rearrangement of propargyloxyanthraquinones to anthrafurandiones in ionic liquids
Nadali, Samaneh,Aghapour, Ghasem,Rafieepour, Zahra
, p. 1045 - 1051 (2017)
An efficient and rapid method is described for the reductive Claisen rearrangement of different propargyloxyanthraquinones to anthra[1,2-b]furan-6,11-diones for first time using iron powder in a mixture of two ionic liquids, namely 1-methylimidazolium tetrafluoroborate [Hmim]BF4 and 1-benzyl-3-methylimidazolium chloride [Bzmim]Cl. The present method is able to execute single or double Claisen rearrangements of 1,4-or 1,5-bispropargyloxyanthraquinones selectively, so that the desired anthra(mono)furandiones or anthra(bis)furandiones are produced, respectively, as the major product.
Experiments directed towards the synthesis of anthracyclinones. V. Double Claisen rearrangement of 1,4-bis(allyloxy)anthraquinones
Cambie,Zhen-Dong,Noall,et al.
, p. 819 - 828 (2007/10/02)
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