Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/85947
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Type: Journal article
Title: A high-yielding enantiospecific synthesis of (-)-7-deoxydaunomycinone
Author: Russell, R.A.
Krauss, A.S.
Warrener, R.N.
Irvine, R.W.
Citation: Tetrahedron Letters, 1984; 25(14):1517-1520
Publisher: Pergamon Press
Issue Date: 1984
ISSN: 0040-4039
1873-3581
Statement of
Responsibility: 
Richard A. Russell, Adrian S. Krauss, Ronald N. Warrener, Robert W. Irvine
Abstract: A comparison is made between two regiospecific modes of base-catalysed condensation of 4 (or 7)-methoxy-3-phenylsulfonyl phthalides with chiral bicyclic quinone monoketals, one of which occurs in 95% yield and forms the basis of the first enantiospecific total synthesis of (−)-7-deoxydaunomycinone (3).
Rights: © 1984 Pergamon Press Ltd.
RMID: 0030009239
DOI: 10.1016/S0040-4039(01)80201-X
Appears in Collections:Chemistry publications

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