Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||A high-yielding enantiospecific synthesis of (-)-7-deoxydaunomycinone|
|Citation:||Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1984; 25(14):1517-1520|
|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.|
|Appears in Collections:||Aurora harvest 2|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.