~~~~~~~~~~~ Letters ~0. 37, pp 3337 - 3338, 1976. Pergamon Press. Printed in Greet Britain.
3337
No. 37
3338
In
the
of
cases
the
obtained in
the
E
and
direct
2
this new method
possibility of synthesizing
pyrimidine
which
gives yields,
of pyrimidines,
oxidation
moreover
l-oxides
this
with
are
higher
than
non-oxidative
substituents
the
method
which
ones opens
up
sensitive
are
for oxidation. Acknowledgement
1.
2.
3.
Pyrimidines
paper
Ring
Transformation
in Reactions
XIII
see
E.A.Oostveen,
in the
press.
H.C.van
der
93,
(1974).
225
5.
R.R.Schmidt,
6.
See
London
for
Tetrahedron
(IWLI); The
and
and
H.C.van
der
Letters
1972,
‘1133;
and
H.C.van
-
spectra
der
Plas,
and
H.Jongejan
“Chemistry
of
the
with
Nucleophiles XIV,
95 (1976),
Rec.TraV.Chim.Pays-Bas
B.Zuurdeeg,
Heterocyclic
for part
=
Kec.Trav.Chim.Pays-Bas
N-oxides",
Academic
Press,
333.
1972,
F.Roeterdink
Compounds
and H.Jongejan,
Plas
J.Minamikawa, Y.Miki, S.Matsugashita and
preparation: Y.Tamura,
their
and H.C.van
p.m.
1971,
Synthesis
C.A.H.Rasmussen
series
of Heterocyclic
J.M.Lagowski,
New York,
lH-NMR, IR
compounds.
these
Miss M.C.Vollering,
Plas,
A.R.Katritzky
in
submitted.
1976,
4.
7.
Previous
LVI.
Rec.Trav.Chim.Pays-Bas
and
K.Kas”ga, der
melting
Plas,
points
M.Hirobe
and T.Okamoto,
Rec.Trav.Chim.Pays-Bas, were
identical
with those
M.Ikeda,
Chem.Pharm.Bull.
2,
submitted.
of
the
authentic
1814