PALLADIUM(0)-CATALYZED ALLYLATION OF URACILS AND THIOURACILS - INFLUENCE OF THE SOLVENT ON THE REGIOSELECTIVITY OF THE ALLYLATION

Citation
C. Goux et al., PALLADIUM(0)-CATALYZED ALLYLATION OF URACILS AND THIOURACILS - INFLUENCE OF THE SOLVENT ON THE REGIOSELECTIVITY OF THE ALLYLATION, Tetrahedron, 52(28), 1996, pp. 9521-9534
Citations number
30
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
52
Issue
28
Year of publication
1996
Pages
9521 - 9534
Database
ISI
SICI code
0040-4020(1996)52:28<9521:PAOUAT>2.0.ZU;2-8
Abstract
Uracil and 5-substituted uracils are monoallylated at N-1 in H2O-CH3CN with the catalytic system Pd(OAch)(2)/P(C6H4-m-SO3Na)(3) (or tppts) a lthough performing the reaction in H2O/THF with the system Pd-2(dba)(3 )/dppb leads to diallylations at N-1 + N-3. 2-Thiouracil, 5-methyl-2-t hiouracil (2-thiothymine) and 6-methyl-2-thiouracil are monoallylated at sulfur in H2O/CH3CN with the catalytic system Pd(OAc)(2)/P(C6H4-m-S O3Na)3 (or tppts). Performing the reactions in H2O/THF with the system Pd-2(dba)(3)/dppb leads to diallylations at N-1 + N-3 of 2-thiouracil and 2-thiothymine whereas 6-methyl-2-thiouracil is diallylated at S N-3. Copyright (C) 1996 Elsevier Science Ltd