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090			_aB-15235
245	1	0	_aExperiments Directed Towards the Synthesis of Anthracyclinones. VIII* Functionalization of Hydroxyanthraquinones by Reductive Claisen Rearrangements
490	0		_vAustralian Journal of Chemistry, 37(7), p.1511-1529, 1984
520	3		_aGentle heating of allyloxyanthraquinones with sodium dithionite in dimethylformamide/water effects a rapid and controlled rearrangement to give high yields of 2-allylhydroxyanthraquinones. Starting from quinizarin, key intermediates for two synthetic routes to 4-demethoxydaunomycinone have been prepared from products by means of two such reductive Claisen rearrangements.
700	1	2	_aBoddy, I.K.
700	1	2	_aBoniface, P.J.
700	1	2	_aCambie, R.C.
700	1	2	_aCraw, P.A.
700	1	2	_aHuang, Z.
700	1	2	_aLarsen, D.S.
700	1	2	_aMcdonald, H.
700	1	2	_aMcdonald, H.
700	1	2	_aWoodgate, P.D.
856	4	0	_uhttps://drive.google.com/file/d/10jurCmOKEws90gfVOnf4f20bU4o4vvVf/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
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